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HERNIA SUPPORTS - EUDAMED Registration 04719863699721

Access comprehensive regulatory information for HERNIA SUPPORTS 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 04719863699721 and manufactured by OPPO Medical Corp. in Taiwan.

This page provides complete registration details including trade name (Hernia Truss with Removable Pad), manufacturer information, authorized representative details, competent authority (DE/CA70 - Landesamt fรผr Umwelt- und Arbeitsschutz), 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
04719863699721
No
HERNIA SUPPORTS
Trade Name: Hernia Truss with Removable Pad
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Device Description (EMDN)

ABDOMINAL HERNIA SUPPORTS

Device Classification
Risk Class
Class I
CND Nomenclatures Code
Y060406
Trade Name
Hernia Truss with Removable Pad
Implantable
No
Reusable
No
Measuring Function
No
Registration Information
Primary DI
04719863699721
Basic UDI
471986369CL110DE
Version Date
December 06, 2024
Manufacturer Last Update
May 26, 2021
Active Status
No
Manufacturer
Manufacturer Name
OPPO Medical Corp.
Country
Taiwan
Country Type
NON_EU
Address
9F, No. 297, Sec. 4, Chung Hsiao East Rd. Taipei
Email
peggylin@oppomedical.com
Authorized Representative
SRN
DE-AR-000000085
Country
Germany
Address
7 Ernst-Heckel-StraรŸe St. Ingbert
Email
ear@mt-procons.com
Telephone
+49 6894 581020
Regulatory Information
Competent Authority
DE/CA70 - Landesamt fรผr Umwelt- und Arbeitsschutz
Applicable Legislation
MDR (REGULATION (EU) 2017/745 on medical devices)
Placed On The Market
Ireland
Device Characteristics
Human Tissues
No
Animal Tissues
No