← Back to catalogue

U Frame

EUDAMED

Class I (EU MDR)

Ref 23001

by Prilanta Surgical

Identity

Trade Name
U Frame EUDAMED
Device Name
U Frame EUDAMED
Model / Reference
23001 EUDAMED

Identifiers

Primary DI / UDI-DI
G54823001 EUDAMED
Basic UDI-DI
++G54823001KE EUDAMED
EMDN Code
Q02100203 METAL AND PLASTIC SPECTACLE FRAMES WITHOUT LENSES EUDAMED

Classification

Device Class
Class I EUDAMED
Market of Registration
Italy 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

U Frame by Prilanta Surgical — Class I — MDR — listed in EUDAMED — regulatory data on deviCERTS

Authorization Coverage (European Union — 27 member states)

Regulatory Authorizations

European Union Active

CE/MDR

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Prilanta Surgical
EUDAMED SRN
PK-MF-000038228
Authorised Representative
ANTEX MEDI SOLUTION DE-AR-000008078

Sources (1)

  • EUDAMED 6df81be3-1120-44d1-b359-b5d869f66264 61 fields · synced Jul 21, 2026