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Drill Guide - EUDAMED Registration D-CNMF0000201150266HM

Access comprehensive regulatory information for Drill Guide 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-CNMF0000201150266HM 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 (DE/CA39, Regierungspräsidium Freiburg Referat 25), 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-CNMF0000201150266HM
No
Drill Guide
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-CNMF0000201150266HM
Basic UDI
B-CNMF0000201150266HM
Version Date
September 20, 2024
Manufacturer Last Update
February 10, 2022
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
DE-AR-000005427
Country
Germany
Address
100 Eisenbahnstrasse Wurmlingen
Email
Mathias.Geml@bricon.com
Telephone
+49 7461 9336 686
Regulatory Information
Competent Authority
DE/CA39, Regierungspräsidium Freiburg Referat 25
Applicable Legislation
MDD (Directive 93/42/EEC on Medical Devices)
Placed On The Market
Spain
Market Available
Portugal:None~None, Spain:None~None
Device Characteristics
Human Tissues
No
Animal Tissues
No