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Procedure Packs - EUDAMED Registration 06973178952782

Access comprehensive regulatory information for Procedure Packs 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 06973178952782 and manufactured by Dongguan Shin Yi Healthcare Products Factory in China.

This page provides complete registration details including manufacturer information, authorized representative details, competent authority (DE/CA22 - Bezirksregierung Münster), 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
06973178952782
No
Procedure Packs
EU EUDAMED Registered Medical Device
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Device Description (EMDN)

SURGICAL PROCEDURAL KITS (EXCLUDING SURGICAL INSTRUMENT KITS)

Device Classification
Risk Class
Class I
CND Nomenclatures Code
T0202
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
06973178952782
Basic UDI
697317895M27T9
Version Date
March 06, 2025
Manufacturer Last Update
June 27, 2024
Active Status
No
Manufacturer
Country
China
Country Type
NON_EU
Address
No. 17 Banhu Rd Dong Guan
Email
zhaosg.dg@master-frank.cn
Authorized Representative
SRN
DE-AR-000000002
Country
Germany
Address
10 Borkstrasse Münster
Email
ecrep@medneteurope.com
Telephone
+49 251 322 66 64
Regulatory Information
Competent Authority
DE/CA22 - Bezirksregierung Münster
Applicable Legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed On The Market
Italy
Device Characteristics
Human Tissues
No
Animal Tissues
No