Pure Global

Razor - EUDAMED Registration 06973911696966

Access comprehensive regulatory information for Razor 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 06973911696966 and manufactured by Finess Healthcare Group Co.,Ltd in China.

This page provides complete registration details including trade name (RAZOR), manufacturer information, authorized representative details, competent authority (Agencia Española de Medicamentos y Productos Sanitarios), 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.

Free Database
Powered by Pure Global AI
EUDAMED Official Data
Class I
06973911696966
No
Razor
Trade Name: RAZOR
Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing
Device Description (EMDN)

BLADES WITH SAFETY SYSTEMS, SINGLE-USE - NOT INCLUDED IN OTHER CLASSES

Device Classification
Risk Class
Class I
CND Nomenclatures Code
V010301
Trade Name
RAZOR
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
06973911696966
Basic UDI
697391169RZ01RH
Version Date
June 17, 2024
Manufacturer Last Update
April 02, 2022
Active Status
No
Manufacturer
Country
China
Country Type
NON_EU
Address
No.1503 A1 Block,No.203 Lantian Road Ningbo
Email
Michelle@finess-healthcare.com
Authorized Representative
SRN
ES-AR-000002008
Country
Spain
Address
141 Pso. Castellana Madrid
Email
legal@zoustech.eu
Regulatory Information
Competent Authority
Agencia Española de Medicamentos y Productos Sanitarios
Applicable Legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed On The Market
France
Device Characteristics
Human Tissues
No
Animal Tissues
No