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Non-sterile Buffing Pad

EUDAMED

Class I (EU MDR)

Ref 6001Model 6002

by Domico Med-Device LLC.

Identity

Device Name
Non-sterile Buffing Pad EUDAMED
Model / Reference
6002 EUDAMED
6001 EUDAMED

Identifiers

Primary DI / UDI-DI
00810050245562 EUDAMED
Basic UDI-DI
081005024TF6002JH EUDAMED
EMDN Code
K0380 ARTHROSCOPY DEVICES, SINGLE USE - ACCESSORIES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Malta 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

Non-sterile Buffing Pad by Domico Med-Device, Llc — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

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Manufacturer

EUDAMED SRN
US-MF-000009144
Authorised Representative
Advena Limited MT-AR-000000234

Sources (1)

  • EUDAMED 1a1c4fa4-07c4-41f4-9f0d-cfae02d5d65b 61 fields · synced Jul 9, 2026