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Mobidisc L

EUDAMED

Class I (EU MDR)

Ref MB900R

by Highridge Medical, LLC.

Identity

Trade Name
MOBIDISC L EUDAMED
Device Name
Forceps EUDAMED
Model / Reference
MB900R EUDAMED

Identifiers

Primary DI / UDI-DI
03662663297950 EUDAMED
Basic UDI-DI
3662663DCT8 EUDAMED
Direct Marketing DI
03662663297950 EUDAMED
EMDN Code
L091103 ORTHOPAEDIC PROSTHESES FORCEPS, REUSABLE EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
France EUDAMED

Clinical & Handling

Sterile

No

EUDAMED

Implantable

No

EUDAMED

Reusable

Yes

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

Mobidisc L by Highridge Medical, 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-000001142
Authorised Representative
LDR Médical FR-AR-000045226

Sources (1)

  • EUDAMED 5031cd68-691a-40e0-aba5-7f4f3f436c7d 61 fields · synced Jun 18, 2026