Search

OVIK Health are innovators who provide exceptional customer care and pioneer advanced technologies to help heal, protect and support. They collaborate to identify unmet needs within the Medical, Sports Medicine, and Animal Health markets to deliver innovative technologies focused on improving care. OVIK Health is a subsidiary of Milliken&Company, a global company active in multiple markets including floor covering, performance and protective textiles, specialty chemicals, healthcare, and operational excellence consulting for industrial manufacturers. Product specification CoFlex TLC CoFlex TLC Zinc & Calamine CoFlex TLC LS The CoFlex TLC difference User friendliness Offers a comprehensive range of products Quick and easy application Promotes safety through consistent application across the range Features EasyTear technology for increased comfort Patient comfort Stays in place Comfortable to wear Adapts to the patient's anatomy Dry dressings minimise itching and odour Zinc / calamine dressings have a soothing effect on irritated skin Allows longer wear time with high evaporation rate. Effective compression Provides therapeutic compression for patient needs With visual indicators to control intended compression On the roll Correctly applied Overstretched Back to prodcuts

Woundcare Products Ligasano epicite hydro Curea Back to products

Contam ® cube Various degrees of prolapse of the vagina and uterus as well as bladder emptying disorders can be treated with the Contam vaginal tampon in the shape of a cube. The flexibility or elasticity of the applied PVA foam allows easy self-treatment. The raw material used for the Contam® vaginal cube is a toxicologically and dermatologically safe foam and has been used for incontinence tampons for decades. Due to the sewn-in removal thread, there is hardly any contact between the thread and the mucous membrane. This prevents irritation. Using instructions Contam cube EN Back to incontinence Back to products

Product specification Application Zurück zur Kompressionstherapie Back to prodcuts

Ligasano is a single-layer polyurethane medical dressing with honeycomb structure, differential porosity and a unique granular surface. It has been used in medicine for over 30 years. All products are CE certified and class IIb according to MDR 2017/745 Ligasano Medikation Ligasano® wound treatment Unlike common polyurethane foams that are normaly used as secondary dressings to absorb and manage exudate, Ligasano is mainly indicated as a primary dressing for debridement and drainage of the woundbed, particularly in chronic and infected wounds. It´s efficacy in debridement and drainage is second only to advanced surgical techniques (eg. Ultrasound, Surgery) and negative pressure wound therapy. However compared to these techniques it´s biomechanical activity is neither expensive nor operator dependent. With it´s peculiar structure and functional properties, Ligasano is a unique dressing that grants an extremely effective and selective debridement, also in case of tunnels and fistulas, while being extremely versatile and economical. How it works Ligasano Ligasano applies a biomechanical action of cleansing the wound bed, that can be divided into 2 subsequent steps: 1. The open-cell surface of Ligasano adheres to the necrotic tissue. The patient's natural movements (walking, breathing, heartbeat, etc.) rattle the honeycombed cell walls and create a slight friction with the wound walls and the wound bed. Unhealthy tissue is thus selectively removed, while underlying healthy, rooted tissue is not damaged. 2. Honeycomb structures react to special physical laws. Under light pressure, the honeycomb cells act like small vacuum pumps and force liquids in the opposite direction. And that is why Ligasano must be lightly pressed into the wound bed. The removed tissue and exudate can flow out of the wound through the Ligasano. Fast, safe and selective. It simply works! Different structures for different applications Ligasano Green Structur LIGASANO® green is an elastic, foamed polyurethane (PUR), almost unhindered by air and water, imaginable like a three-dimensional sieve. The structure is coarse, the surface rough. Application Extremely high drainage, significant mechanical hard debridement capacity, considerable stimulation of the proliferative phase, insignificant absorption and thermohygrometric capabilities . Indication Primary dressing for hard debridement of chronic and/or infected wounds, debridement of radicated fibrinuous sediments, slough and necrotic tissues. Drainage and cleansing of heavily suppurating lesions, even with highly dense exudate. To be used in contact with necrotic and spurious tissues, and fibrinous sediments. Avoid contact with delicate tissues (tendons, bones, primary blood vessels, intestines) and healthy perilesional skin . Using instructions Ligasano green Ligasano White Structure LIGASANO® white has mixed pores, i.e. it has open, half-open and closed pores Application Strong drainage, high permeability, good mechanical debridement capacity (soft debridement) and stimulation of granulating tissues. Absorption capacities up to 88% of it´s volume and mantainance of thermohygrometric equilibriume. Indications Primary dressing for soft debridement (biofilm, slough, fibrinous sediments) of chronic and/or infected wounds. Drainage of moderately suppurating lesions with exudate of low average density. May be used in contact with delicate tissues and healthy and perilesional skin. Secondary dressing specifically indicated for infected wounds, where a highly permeabel dressing is required to control the bacterial load, opposed to other situations in which the managing of high volume of exudate in low bacterial load conditions ist he priority. Using instructions Ligasano white Back to Ligasano Indications Variants of treatment of pressure ulcers category 3 Ulcer treatment in the ankle or lower leg area Back to the products

Exsudate management for malodourous wounds P1 DUO active P2 active Curea P1 DUO active Exudate management, soft debridement and odour reduction with a single wound dressing curea active wound dressings quickly relieve nagging wound odour and thus improve the quality of life for patients and their relatives. In addition, they bind bacteria in a purely physical way and are therefore also excellent for fighting infections. curea P1 duo active fights and neutralises wound odours quickly with its integrated activated charcoal layer. In infected wounds, it also reduces germs through purely physical means, without the risk of developing antimicrobial resistance. Integrated activated charcoal layer for very good odour absorption even in the case of extremely strong wound odours Reduction of the bacterial microbial load in the wound without the risk of microbial resistance and cytotoxicity Cleansing effect with regard to exo- and endotoxins High absorption even under compression and pressure SuperCore® ensures secure binding of excessive exudate Binding and reduction of germs and MMPs Blood binding Soft debridement during dressing changes Reduced risk of wound maceration Core remains stable during application Maintains a balanced, moist wound environment Wear time up to 7 days Indication for use: Slightly to heavily exuding wounds malodorous chronic and acute wounds Infected wounds and wounds at risk of infection IFU P1 Curea P1 DUO active IFU Curea P2 active SuperCore®, activated charcoal and wound spacer grid in one powerful product. Exudate, wound odour, wound infections, and pain during dressing changes are no challenge with curea P2 active and can be treated simultaneously with the wound dressing - without the need for costly sandwich dressings. Document Curea P2 active IFU Back to Curea Back to products

PPE-Products Our articles are high-quality, certified products that guarantee protection and safety. Together for safety, because your health is important to us. Antigentests - professional Flowflex SARS-Cov-2- rapid antigentest A rapid test for the qualitative detection of SARS-CoV2 nucleocapsid antigens in nasal and nasopharyngeal swab specimens. Materials provided: 25 test cassettes: each test cassette packed in foil pouches with desiccant. 25 Exraction Buffer Tubes 25 Sterilised swabs: Disposable swabs for specimen collection. Postitive/negative control - 1 stick each 1 workstation 1 package insert The test may only be performed by healthcare professionals or specially trained professionals Certification: DIN EN ISO 13485:2016 - In-vitro-Diagnostic RL 98/79/EG Annex 3 Flowflex SARS-Cov-2- rapid antigen test A rapid test for the qualitative detection of SARS-CoV2 nucleocapsid antigens in nasal and nasopharyngeal swab specimens. Materials provided: 20 test cassettes: each test cassette packed in foil pouches with desiccant. 20 Exraction Buffer Tubes 20 Sterilised swabs: Disposable swabs for nasal sampling 20 Sterilised swabs: disposable swabs for nasopharyngeal sampling 1 package insert The test may only be performed by healthcare professionals or specially trained professionals! Certification: DIN EN ISO 13485:2016 - In-vitro-Diagnostic RL 98/79/EG Annex 3 Antigentests - self testing Flowflex SARS-Cov-2 Rapid Antigen Test (Self-Test) A rapid test for the qualitative detection of SARS-CoV2 nucleocapsid antigens in anterior nasal swab specimens. Package sizes: Single test, 5 tests, 25 tests Materials provided: Test cassettes: each test cassette packed in foil pouch with desiccant. Extraction buffer tubes Sterilised swabs: Disposable swabs for nasal sampling Waste bags 1 package insert Certification DIN EN ISO 13485:2016 - In-vitro-Diagnostics RL 98/79/EG Annex 3 to the shop Back to PPE Products Back to Products

Wound dressings Products Exudate management and Soft Debridement Exudate management for sensitive skin Exudate management for malodorous wounds Video Curea Video die Kraft der Curea Wundauflage Curea Video EN the power of Curea dressings Video Curea Active DE Video Curea Active EN Back to prodcuts

Chronic wounds Direct insight into how it works Here you will get an insight into the treatment methods for various wound healing supplies. Case report 1 - decubitus on the rump with wet necrosis Patient data and anamnesis: Pressure sores on the rump with wet necrosis on an 89-year-old, completely immobile patient. There is also diabetes mellitus with high blood sugar levels and MRSA infection. The patient is only partially oriented and capable of contact. For some weeks mobilization in the wheelchair is only occasionally possible. The care and nursing takes place via an outpatient nursing service 3 times a day and a home care service instead. The patient lies on a alternating pressure system and is stored. The urine excretion is passed through a urostoma. There is a fecal incontinence with frequent stool frequencies. So far, the decubitus was performed with a fine-pored foam dressing in three-day rhythm. This treatment resulted in no result. Exudate levels are moderate Fig. 1: 02.02.2016 Fig. 1: 10.02.2016 Fig. 1: 02.02.2016 Fig. 1: 19.02.2016 Fig. 1: 02.02.2016 Fig. 1: 09.03.2016 Fig. 1: 02.02.2016 Initially, a mechanical wound cleaning with polyhexanide solution and LIGASANO® intensive and soft was performed. Fig. 2: 02.02.2016 Tamponade of the small undermining at 3 o'clock and covering of the wound surface with LIGASANO® white wound strip mini. Fig. 3: 02.02.2016 Covering the wound area with LIGASANO® white sterile 15 x 10 x 1 cm and 24 x 16 x 1 cm. Fixation with adhesive fleece at the margin area. Dressing change every two days. In support of this, the patient was stored on LIGASANO® green 55 x 45 x 2 cm and LIGASANO® white 59 x 49 x 2 cm. Fig. 4: 10.02.2016 Further mechanical wound cleaning with polyhexanide solution and LIGASANO® intensive and soft. Complete replacement of necrosis by LIGASANO® alone. Fig. 5: 19.02.2016 The moist necroses and coatings were increasingly removed by the treatment with LIGASANO® white. This results in an increase in wound depth. The surrounding skin with the smaller decubitus ulcers has calmed significantly and the lesions have healed. The treatment is continued with the LIGASANO® white wound strip mini, the cover of the wound surface with LIGASANO® white sterile 15 x 10 x 1 cm and additionally with LIGASANO® white sterile 24 x 16 x 1 cm. Fixation with adhesive fleece at the margin area. Dressing change every two days. Fig. 6: 09.03.2016 The entire surrounding skin is intact and non-irritant. The wound bed has cleared and shows granulation islands. Significant decrease in wound depth through granulation. Author: Daniela Laskowski, nurse, wound expert from Fulda, correspondence through LIGAMED® medical Produkte Gmb (c) Ligamed Back to applications Back to the products

Privacy policy In the following data protection declaration we inform you about the most important aspects of data processing within the framework of our website. We collect and process personal data only on the basis of the legal provisions (Basic Data Protection Regulation, Telecommunications Act 2003). As soon as you access or visit our website as a user, your IP address, start and end of the session are recorded. This is for technical reasons and therefore constitutes a legitimate interest within the meaning of Art. 6 Para. 1 lit. f DSGVO. Contact us If you contact us, either via our contact form on our website or by email, the data you send us will be stored by us for six months for the purpose of processing your enquiry or in the event of further follow-up questions. Your transmitted data will not be passed on without your consent. Data storage Within the scope of facilitating the shopping process and for the subsequent processing of the contract, the IP address of the connection owner is stored by the webshop operator within the scope of cookies, as are the name, delivery and invoice address, and ATU number if applicable. The following data is also stored by us for the purpose of contract processing: Email, telephone number. The data provided by you is necessary for the fulfilment of the contract and for the implementation of pre-contractual measures. It is not possible to conclude a contract without this data. The data collected is not transmitted to third parties, with the exception of the transmission of payment data (credit card data) to the processing bank/payment service provider for the purpose of debiting the purchase price, to the shipping company (transport company) commissioned by us to deliver the goods and to our tax advisor for the purpose of fulfilling our obligations under tax law. If you cancel the purchase process, the data stored by us will be deleted. Should a contract be concluded, all data resulting from the contractual relationship will be stored until the expiry of the retention period required by tax law (7 years). The transmitted name, address, purchased goods and date of purchase will also be stored until the expiry of product liability (10 years). The data processing is carried out on the basis of the legal provisions of § 96 para 3 TKG as well as Art 6 para 1 lit a (consent) and/or lit b (necessary for the fulfilment of the contract) of the DSGVO. Cookies Our website uses so-called cookies. These are small text files that are stored on your end device with the help of the browser. They do not cause any damage. We use cookies to make our offer user-friendly. Some cookies remain stored on your end device until you delete them. They enable us to recognise your browser on your next visit. If you do not wish this, you can set your browser so that it informs you about the setting of cookies and you only allow this in individual cases. If you deactivate cookies, the functionality of our website may be limited. Your rights As a data subject, you have a fundamental right with regard to your data stored by us to: Information Deletion of data Transferability of data Revocation and objection to data processing. If you suspect that violations of data protection law have occurred in the course of processing your data, you have the possibility to complain to us (info(at)sini-medik.com) or to the data protection authority. You can reach us at the following contact details: SINI-MEDIK Niederreiter GmbH Email: info(at)sini-medik.com Telefon: +43 5412 61892 Quelle: Erstellt mit dem Datenschutz-Generator von AdSimple

Biotechnology - Extremities OASIS® Extracellular Matrix Cook Biotech’s advanced tissue-repair products are derived from porcine small intestinal submucosa (SIS) and other ECM-based biomaterials. They are used to manage multiple types of wounds, including burns, diabetic ulcers, venous ulcers, and trauma wounds. Surgical applications include hernia repair, fistula repair, otologic repair, and soft-tissue reinforcement. Document OASIS Instruction for use up Video Oasis OASIS Brochure EN Back to Biotechnologie Back to products

Biotechnologie - Pelvis 4layer Fistula plug Rectopexy OASIS ECM Biodesign® 4 Layer Tissue The Biodesign 4-Layer Tissue Graft is intended for implantation to reinforce soft tissue. It is indicated for use in chordee correction, Peyronie’s disease treatment, and urethral repair. Document Document Document 4 Layer Instructions Biodesign Breadth of offering Biodesign scientific monograph 4layer Biodesign® Fistula Plug - not available at the moment! The Biodesign Fistula Plug is for implantation to reinforce soft tissue for repair of anorectal fistulas. Document Document Document OASIS Instruction for use Biodesign Breadth of offering EN Biodesign scientific monograph Up Video Fistula Plug Biodesign® Fistula Plug The Biodesign Fistula Plug is for implantation to reinforce soft tissue for repair of anorectal fistulas. Fistula Biodesign® Rectopexy Graft The Biodesign Rectopexy Graft is intended to support/reinforce soft tissue in surgical procedures for open and laparoscopic repair of rectal prolapse/rectal intussusception. Document Rectopexy Graft Instruction for use Document Biodesign Breadth of offering EN Document Biodesign scientific monograph Recto OASIS® Extracellular Matrix Cook Biotech’s advanced tissue-repair products are derived from porcine small intestinal submucosa (SIS) and other ECM-based biomaterials. They are used to manage multiple types of wounds, including burns, diabetic ulcers, venous ulcers, and trauma wounds. Surgical applications include hernia repair, fistula repair, otologic repair, and soft-tissue reinforcement. Document OASIS Instruction for use up Video Oasis OASIS Brochure EN OASIS Back to Biotechnology Back to prdoucts