Vilowond® Gauze & Vilowond® Nonwoven
- Risk class
- Class I
- CND nomenclatures code
- M0201020101
- Trade name
- Vilowond®Gauze Non-Sterile
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 06221329007059
- Basic UDI
- 62220238VilowondGNWBP
- Version date
- May 30, 2024
- Manufacturer last update
- May 18, 2021
- Active status
- No
- Manufacturer name
- Pharmaplast
- Country
- Egypt
- Country type
- NON_EU
- Address
- Amria free zone Alexandria
- ra@pharmaplast-online.com
- Name
- E C REP LIMITED
- SRN
- IE-AR-000003995
- Country
- Ireland
- Address
- 5 Fitzwilliam Square East Dublin D2
- info@ecrep.ie
- Telephone
- +353 89 225 1951
- Competent authority
- Health Products Regulatory Authority, Medical Devices Department
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- United Kingdom (Northern Ireland only)
- Market available
- Austria:None~None, Belgium:None~None, Bulgaria:None~None, Croatia:None~None, Cyprus:None~None, Czechia:None~None, Denmark:None~None, Estonia:None~None, Finland:None~None, France:None~None, Germany:None~None, Greece:None~None, Hungary:None~None, Iceland:None~None, Ireland:None~None, Italy:None~None, Latvia:None~None, Liechtenstein:None~None, Lithuania:None~None, Luxembourg:None~None, Malta:None~None, Netherlands:None~None, Norway:None~None, Poland:None~None, Portugal:None~None, Romania:None~None, Slovakia:None~None, Slovenia:None~None, Spain:None~None, Sweden:None~None, Türkiye:None~None, United Kingdom (Northern Ireland only):None~None
- Human tissues
- No
- Animal tissues
- No
COTTON GAUZES, FOLDED, WITHOUT X-RAY DETECTABLE THREAD, STERILE
Access comprehensive regulatory information for Vilowond® Gauze & Vilowond® Nonwoven in the European Union medical device market through Pure Global AI's free database. This Class I device is registered with EU EUDAMED under Primary DI 06221329007059 and manufactured by Pharmaplast in Egypt.
This page provides complete registration details including trade name (Vilowond®Gauze Non-Sterile), manufacturer information, authorized representative details, competent authority (Health Products Regulatory Authority, Medical Devices Department), and regulatory compliance data from the official EU EUDAMED medical device database. Pure Global AI offers free access to the European Union's complete medical device registry, helping global MedTech companies navigate EU MDR regulations efficiently.