Procedure Packs
- Risk class
- Class I
- CND nomenclatures code
- T0202
- Implantable
- No
- Reusable
- No
- Measuring function
- No
- Primary DI
- 06973178952720
- Basic UDI
- 697317895M21SV
- Version date
- March 06, 2025
- Manufacturer last update
- June 27, 2024
- Active status
- No
- Manufacturer name
- Dongguan Shin Yi Healthcare Products Factory
- Country
- China
- Country type
- NON_EU
- Address
- No. 17 Banhu Rd Dong Guan
- zhaosg.dg@master-frank.cn
- SRN
- DE-AR-000000002
- Country
- Germany
- Address
- 10 Borkstrasse Münster
- ecrep@medneteurope.com
- Telephone
- +49 251 322 66 64
- Competent authority
- DE/CA22 - Bezirksregierung Münster
- Applicable legislation
- MDR (REGULATION (EU) 2017/745 on medical devices)
- Placed on the market
- Italy
- Human tissues
- No
- Animal tissues
- No
SURGICAL PROCEDURAL KITS (EXCLUDING SURGICAL INSTRUMENT KITS)
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 06973178952720 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.