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EUDAMED registration 06942272682192No

Adhesive Plaster

FIRSTAR HEALTHCARE COMPANY LlMITED(GUANGZHOU)Class IEU EUDAMEDTrade name: PLASTER DRESSING/Adhesive Plaster
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class I
CND nomenclatures code
M04010199
Trade name
PLASTER DRESSING/Adhesive Plaster
Implantable
No
Reusable
No
Measuring function
No
Registration information
Primary DI
06942272682192
Basic UDI
69422726P2.02.11WM
Version date
March 05, 2025
Manufacturer last update
July 13, 2021
Active status
No
Manufacturer
Manufacturer name
FIRSTAR HEALTHCARE COMPANY LlMITED(GUANGZHOU)
Country
China
Country type
NON_EU
Address
Rm. 901, Building No.2, Headquarters Center, Tian'an High-tech EcologicalPark, Panyu, PEOPLE'S REPUBLIC OF CHINA Guangzhou
Email
Yan@firstar.cc
Authorized representative
Name
MedPath GmbH
SRN
DE-AR-000000087
Country
Germany
Address
8 Mies-van-der-Rohe-Strasse Munich
Email
info@medpath.pro
Telephone
+49 (0) 89 8130 6837
Regulatory information
Competent authority
DE/CA304 - Marktüberwachung Medizinprodukte Bayern
Applicable legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed on the market
Germany
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

ADHESIVE DRESSINGS, WITH ABSORBENT PAD - OTHER

About this record

Access comprehensive regulatory information for Adhesive Plaster 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 06942272682192 and manufactured by FIRSTAR HEALTHCARE COMPANY LlMITED(GUANGZHOU) in China.

This page provides complete registration details including trade name (PLASTER DRESSING/Adhesive Plaster ), manufacturer information, authorized representative details, competent authority (DE/CA304 - Marktüberwachung Medizinprodukte Bayern), 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.