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Hemostasis Valve - EUDAMED Registration 06945764406757

Access comprehensive regulatory information for Hemostasis Valve 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 06945764406757 and manufactured by Shenzhen Antmed Co., Ltd in China.

This page provides complete registration details including trade name (Hemostasis Valve), manufacturer information, authorized representative details, competent authority (DE/CA22 - Bezirksregierung Münster), 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
06945764406757
No
Hemostasis Valve
Trade Name: Hemostasis Valve
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Device Description (EMDN)

HAEMOSTASIS VALVES

Device Classification
Risk Class
Class I
CND Nomenclatures Code
C900101
Trade Name
Hemostasis Valve
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
06945764406757
Basic UDI
69457644HV00000007ZV
Version Date
January 09, 2025
Manufacturer Last Update
August 07, 2024
Active Status
No
Manufacturer
Manufacturer Name
Shenzhen Antmed Co., Ltd
Country
China
Country Type
NON_EU
Address
18 Jinhui Ave., Pingshan New District 518122 Shenzhen
Email
info@antmed.com
Authorized Representative
SRN
DE-AR-000011194
Country
Germany
Address
10 Borkstrasse Münster
Email
contact@mednet-ecrep.com
Regulatory Information
Competent Authority
DE/CA22 - Bezirksregierung Münster
Applicable Legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed On The Market
Germany
Market Available
France:None~None, Germany:None~None
Device Characteristics
Human Tissues
No
Animal Tissues
No