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Hip Pack - EUDAMED Registration 06975197845304

Access comprehensive regulatory information for Hip Pack 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 06975197845304 and manufactured by Leboo (Hubei) Healthcare Products Limited in China.

This page provides complete registration details including manufacturer information, authorized representative details, competent authority (DE/CA20, Bezirksregierung Düsseldorf Dezernat 24), 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
06975197845304
No
Hip Pack
EU EUDAMED Registered Medical Device
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Device Description (EMDN)

SURGICAL PROCEDURAL KITS (EXCLUDING SURGICAL INSTRUMENT KITS)

Device Classification
Risk Class
Class I
CND Nomenclatures Code
T0202
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
06975197845304
Basic UDI
697519784Z53WU
Active Status
No
Manufacturer
Country
China
Country Type
NON_EU
Address
No. 18 Tianxian Street,Tianmen Industrial Park,Tianmen City,431748 Hubei,P.R.China Tianmen Hubei
Email
Nita@leboochina.com.cn
Authorized Representative
SRN
DE-AR-000005132
Country
Germany
Address
83 Heerdter Lohweg Düsseldorf
Email
eu-rep@share-info.com
Regulatory Information
Competent Authority
DE/CA20, Bezirksregierung Düsseldorf Dezernat 24
Applicable Legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed On The Market
Netherlands
Device Characteristics
Human Tissues
No
Animal Tissues
No