Hydrocolloid blister plaster
- Risk class
- Class IIa
- CND nomenclatures code
- M04040301
- Trade name
- Hydrocolloid blister plaster
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 06926365595118
- Basic UDI
- 69263655200057Y
- Version date
- January 20, 2025
- Manufacturer last update
- July 17, 2023
- Active status
- No
- Manufacturer name
- Zhejiang Longterm Medical Technology Co., Ltd.
- Country
- China
- Country type
- NON_EU
- Address
- ShuangShan Road 277,FuXi Street ,Deqing County 313200 Huzhou City,Zhejiang Deqing, Zhejiang
- rachel@longterm-health.com
- Name
- Lotus NL B.V.
- SRN
- NL-AR-000000121
- Country
- Netherlands
- Address
- Koningin Julianaplein 10, 1e Verd The Hague
- info@lotusnl.com
- Competent authority
- Ministerie van Volksgezondheid, Welzijn en Sport
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- France
- Market available
- France:None~None
- Human tissues
- No
- Animal tissues
- No
HYDROCOLLOID DRESSINGS, NON-COMBINED
Access comprehensive regulatory information for Hydrocolloid blister plaster in the European Union medical device market through Pure Global AI's free database. This Class IIa device is registered with EU EUDAMED under Primary DI 06926365595118 and manufactured by Zhejiang Longterm Medical Technology Co., Ltd. in China.
This page provides complete registration details including trade name (Hydrocolloid blister plaster), manufacturer information, authorized representative details, competent authority (Ministerie van Volksgezondheid, Welzijn en Sport), 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.