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Eyevan

EUDAMEDFDA UDI

Class I (EU MDR)

Ref CADET(49)-E 49 TORTModel Plastic

by EYEVAN Inc.

Identity

Trade Name
EYEVAN EUDAMEDFDA UDI
Generic Name
Spectacle frame FDA UDI
Device Name
Plastic spectacle frames without lenses EUDAMED
Model / Reference
Plastic EUDAMED
CADET(49)-E 49 TORT EUDAMEDFDA UDI

Identifiers

Primary DI / UDI-DI
04582667993292 EUDAMEDFDA UDI
Basic UDI-DI
458266799RXPLAW8 EUDAMED
FDA Product Code
HQZ FDA UDI
EMDN Code
Q02100202 PLASTIC SPECTACLE FRAMES WITHOUT LENSES EUDAMED
GMDN Term
Spectacle frame FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
886.5842 FDA UDI
Market of Registration
France EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

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

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Eyevan by Eyevan Inc. — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
EYEVAN Inc.
EUDAMED SRN
JP-MF-000028437
Authorised Representative
EYEVAN Europe FR-AR-000025678

Sources (2)

  • EUDAMED 91cd3b6a-fbbc-4a3f-8cc9-3ba8020df164 61 fields · synced Jul 15, 2026
  • FDA UDI 49369fb9-e111-4186-868c-82caff06564b 32 fields · synced May 30, 2026