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Portable Sampling Booth - EUDAMED Registration 16975281480029

Access comprehensive regulatory information for Portable Sampling Booth 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 16975281480029 and manufactured by Shenzhen Relicare Medical Co., Ltd. in China.

This page provides complete registration details including trade name (Portable Sampling Booth), manufacturer information, authorized representative details, competent authority (Agencia Espaรฑola 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.

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EUDAMED Official Data
Class I
16975281480029
No
Portable Sampling Booth
Trade Name: Portable Sampling Booth
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Device Description (EMDN)

HEALTH SERVICE PREMISES PROTECTION DEVICES - OTHER

Device Classification
Risk Class
Class I
CND Nomenclatures Code
T030599
Trade Name
Portable Sampling Booth
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
16975281480029
Basic UDI
697528148PSBoothTCA001SZ
Version Date
July 03, 2022
Manufacturer Last Update
June 21, 2022
Active Status
No
Manufacturer
Country
China
Country Type
NON_EU
Address
N/A Room 416, Building 2, Shenzhen New Generation Industrial Park, No. 136, Zhongkang Road, Meidu Community, Meilin Street, Futian District Shenzhen
Email
wudongping@relicaremed.com
Authorized Representative
SRN
ES-AR-000002008
Country
Spain
Address
141 Paseo de la Castellana Madrid
Email
legal@zoustech.eu
Regulatory Information
Competent Authority
Agencia Espaรฑola de Medicamentos y Productos Sanitarios
Applicable Legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed On The Market
Germany
Device Characteristics
Human Tissues
No
Animal Tissues
No