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Mtl

EUDAMED

Class A (EU MDR)

Ref MTL02AB69

by Appolon Bioteck

Identity

Trade Name
MTL EUDAMED
Device Name
MTL EUDAMED
Model / Reference
MTL02AB69 EUDAMED

Identifiers

Primary DI / UDI-DI
03760322820027 EUDAMED
Basic UDI-DI
376032282APANMTLD8 EUDAMED
EMDN Code
W050299 DEVICES FOR SAMPLES TRANSPORT - OTHER EUDAMED

Classification

Device Class
Class A EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Microbial Substances

No

EUDAMED

Reagent

Yes

EUDAMED

Self Testing

No

EUDAMED

Near-Patient Testing

No

EUDAMED

Professional Testing

Yes

EUDAMED

Companion Diagnostics

No

EUDAMED

Surgical Instrument

No

EUDAMED

New Device

No

EUDAMED

Category: General specimen container IVD, no additive/medium

Mtl by Appolon Bioteck — Class A — IVDR — listed in EUDAMED — regulatory data on deviCERTS

Similar devices

Also classified as General specimen container IVD, no additive/medium.

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/IVDR

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Manufacturer

Manufacturer
Appolon Bioteck
EUDAMED SRN
FR-MF-000022234

Sources (1)

  • EUDAMED f5f8c9de-c82e-42bc-9424-9700e011e529 61 fields · synced Jul 9, 2026