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Tynor

EUDAMED

Class I (EU MDR)

Ref I 59

by Tynor Orthotics Pvt Ltd

Identity

Trade Name
Tynor EUDAMED
Device Name
Abdominal Hernia Support EUDAMED
Model / Reference
I 59 EUDAMED

Identifiers

Primary DI / UDI-DI
08903424115058 EUDAMED
Basic UDI-DI
8903424AHD031299C7 EUDAMED
Direct Marketing DI
08903424115058 EUDAMED
EMDN Code
Y060406 ABDOMINAL HERNIA SUPPORTS EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Denmark EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

No

EUDAMED

Contains Latex

No

EUDAMED

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Category: Abdominal hernia truss, reusable

Tynor by Tynor Orthotics Pvt Ltd — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as Abdominal hernia truss, reusable.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
IN-MF-000005705
Authorised Representative
Medical Technology Promedt Consulting GmbH DE-AR-000000085

Sources (1)

  • EUDAMED 63f540f3-2c58-4d59-8169-37e7bfeec2f3 61 fields · synced Jun 18, 2026