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EMERGENCY BLANKET - EUDAMED Registration 16942272601343

Access comprehensive regulatory information for EMERGENCY BLANKET 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 16942272601343 and manufactured by FIRSTAR HEALTHCARE COMPANY LlMITED(GUANGZHOU) in China.

This page provides complete registration details including trade name (EMERGENCY BLANKET), manufacturer information, authorized representative details, competent authority (DE/CA304 - Marktรผberwachung 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.

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EUDAMED Official Data
Class I
16942272601343
No
EMERGENCY BLANKET
Trade Name: EMERGENCY BLANKET
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Device Description (EMDN)

DEVICES FOR BODY PROTECTION - OTHER

Device Classification
Risk Class
Class I
CND Nomenclatures Code
Y090699
Trade Name
EMERGENCY BLANKET
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
16942272601343
Basic UDI
69422726P3.03.01XA
Version Date
February 06, 2025
Manufacturer Last Update
July 13, 2021
Active Status
No
Manufacturer
Country
China
Country Type
NON_EU
Address
Rm. 901, Building No.2, Headquarters Center, Tian'an High-tech EcologicalPark, Panyu, PEOPLE'S REPUBLIC OF CHINA Guangzhou
Email
Yan@firstar.cc
Authorized Representative
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 - Marktรผberwachung 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