Pure Global AI
EUDAMED registration 06973137576424No

Combined external fixator

Beijing Ruibaoli Medical Equipment Co., Ltd.Class IEU EUDAMEDTrade name: Combined external fixator
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class I
CND nomenclatures code
P09120499
Trade name
Combined external fixator
Implantable
No
Reusable
No
Measuring function
No
Registration information
Primary DI
06973137576424
Basic UDI
697313757642L8
Version date
January 14, 2025
Manufacturer last update
June 13, 2024
Active status
No
Manufacturer
Manufacturer name
Beijing Ruibaoli Medical Equipment Co., Ltd.
Country
China
Country type
NON_EU
Address
No.101, Building 1, Courtyard 6, Hengye north seventh street, Tongzhou District Beijing
Email
xz@bjruibaoli.com
Authorized representative
Name
MedPath GmbH
SRN
DE-AR-000000087
Country
Germany
Address
8 Mies-van-der-Rohe-Strasse Munich
Email
info@medpath.pro
Telephone
+49 (0) 89 8130 6837
Regulatory information
Competent authority
DE/CA304 - Marktüberwachung Medizinprodukte Bayern
Applicable legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed on the market
Germany
Device characteristics
Human tissues
No
Animal tissues
No
Device description (EMDN)

EXTERNAL BONE FIXATION SYSTEMS - OTHER

About this record

Access comprehensive regulatory information for Combined external fixator 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 06973137576424 and manufactured by Beijing Ruibaoli Medical Equipment Co., Ltd. in China.

This page provides complete registration details including trade name (Combined external fixator), manufacturer information, authorized representative details, competent authority (DE/CA304 - Marktüberwachung Medizinprodukte Bayern), 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.