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EUDAMED registration 06977728545738Yes

Electric Ambulance Stretcher

Suzhou Ireland Medical Equipment Co., Ltd.Class IEU EUDAMEDTrade name: Electric Ambulance Stretcher
VerifiedEUDAMED · official EU database
Device classification
Risk class
Class I
CND nomenclatures code
V08050102
Trade name
Electric Ambulance Stretcher
Implantable
No
Reusable
No
Measuring function
No
Registration information
Primary DI
06977728545738
Basic UDI
697772854DWEASVJ
Version date
September 24, 2024
Manufacturer last update
September 12, 2024
Active status
Yes
Manufacturer
Manufacturer name
Suzhou Ireland Medical Equipment Co., Ltd.
Country
China
Country type
NON_EU
Address
Building E, Liangfeng Machinery Park, No.3 Zhenxing Road, Yangshe Town Zhangjiagang City
Email
provider@dragon-iec.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)

SELF-LOADING STRETCHERS

About this record

Access comprehensive regulatory information for Electric Ambulance Stretcher 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 06977728545738 and manufactured by Suzhou Ireland Medical Equipment Co., Ltd. in China.

This page provides complete registration details including trade name (Electric Ambulance Stretcher), 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.