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Inner Drill Sleeve - EUDAMED Registration D-CNMF0000201151409HS

Access comprehensive regulatory information for Inner Drill Sleeve 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 D-CNMF0000201151409HS and manufactured by Tianjin Zhengtian Medical Instrument Co., Ltd. in China.

This page provides complete registration details including manufacturer information, authorized representative details, competent authority (Finnish Medicines Agency, Supervision and licences, Medical Device Unit), 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
D-CNMF0000201151409HS
No
Inner Drill Sleeve
EU EUDAMED Registered Medical Device
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Device Description (EMDN)

ORTHOPAEDIC PROSTHESES POSITIONERS, REUSABLE

Device Classification
Risk Class
Class I
CND Nomenclatures Code
L091104
Implantable
No
Reusable
Yes
Measuring Function
No
Registration Information
Primary DI
D-CNMF0000201151409HS
Basic UDI
B-CNMF0000201151409HS
Version Date
March 10, 2025
Manufacturer Last Update
February 12, 2025
Active Status
No
Manufacturer
Country
China
Country Type
NON_EU
Address
No.318, Jingyi Road, Airport Economic Zone Tianjin
Email
info@natongroup.com
Authorized Representative
SRN
FI-AR-000046224
Country
Finland
Address
2 Lääkärinkatu Tampere
Email
info@inion.com
Regulatory Information
Competent Authority
Finnish Medicines Agency, Supervision and licences, Medical Device Unit
Applicable Legislation
MDD (Directive 93/42/EEC on Medical Devices)
Placed On The Market
Portugal
Market Available
Portugal:None~None, Spain:None~None
Device Characteristics
Human Tissues
No
Animal Tissues
No