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Endotracheal Tube - EUDAMED Registration D-ETT5011XT

Access comprehensive regulatory information for Endotracheal Tube in the European Union medical device market through Pure Global AI's free database. This Class IIa device is registered with EU EUDAMED under Primary DI D-ETT5011XT and manufactured by Hangzhou Tappa Medical Technology Co , Ltd. in China.

This page provides complete registration details including trade name (Endotracheal Tube), 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 IIa
D-ETT5011XT
No
Endotracheal Tube
Trade Name: Endotracheal Tube
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Device Description (EMDN)

ENDOTRACHEAL TUBES, CUFFLESS, NOT REINFORCED

Device Classification
Risk Class
Class IIa
CND Nomenclatures Code
R01030101
Trade Name
Endotracheal Tube
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
D-ETT5011XT
Basic UDI
B-ETT5011XT
Version Date
November 18, 2022
Manufacturer Last Update
December 08, 2022
Active Status
No
Manufacturer
Country
China
Country Type
NON_EU
Address
No.225 Chutian Rd. Binjiang District Hangzhou
Email
hr@tappamed.cn
Authorized Representative
SRN
DE-AR-000005129
Country
Germany
Address
56 Brehmstr Düsseldorf
Email
med@eulinx.eu
Telephone
+4921131054698
Regulatory Information
Competent Authority
DE/CA20, Bezirksregierung Düsseldorf Dezernat 24
Applicable Legislation
MDD (Directive 93/42/EEC on Medical Devices)
Placed On The Market
Germany
Market Available
Germany:2021-02-26~2024-05-26
Device Characteristics
Human Tissues
No
Animal Tissues
No