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Non woven swabs - EUDAMED Registration 06941558088635

Access comprehensive regulatory information for Non woven swabs 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 06941558088635 and manufactured by Allmed Medical Products Co.,Ltd in China.

This page provides complete registration details including manufacturer information, authorized representative details, competent authority (DE/CA05 - Behorde fur Justiz und Verbraucherschutz), 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.

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EUDAMED Official Data
Class I
06941558088635
No
Non woven swabs
EU EUDAMED Registered Medical Device
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Device Description (EMDN)

NON-WOVEN GAUZE PADS, WITHOUT X-RAY DETECTABLE THREAD, STERILE

Device Classification
Risk Class
Class I
CND Nomenclatures Code
M0202030101
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
06941558088635
Basic UDI
69415580nonwovswabEOIsYC
Version Date
February 27, 2025
Manufacturer Last Update
June 22, 2021
Active Status
No
Manufacturer
Country
China
Country Type
NON_EU
Address
No.18 Qixing Road 443200 Zhijiang city, Hubei province
Email
sale@allmed.cn
Authorized Representative
SRN
DE-AR-000000001
Country
Germany
Address
80 Eiffestraße Hamburg
Email
shholding@hotmail.com
Telephone
+49 40 2513175
Regulatory Information
Competent Authority
DE/CA05 - Behorde fur Justiz und Verbraucherschutz
Applicable Legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed On The Market
Germany
Device Characteristics
Human Tissues
No
Animal Tissues
No