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C-Quant

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 80000

by OCULUS Optikgeräte GmbH

Identity

Trade Name
C-Quant EUDAMEDFDA UDI
Generic Name
Binocular vision test unit FDA UDI
Device Name
C-Quant EUDAMEDFDA UDI
Model / Reference
80000 EUDAMEDFDA UDI
Description
C-Quant FDA UDI

Identifiers

Primary DI / UDI-DI
04049584014795 EUDAMEDFDA UDI
Basic UDI-DI
404958414PU EUDAMED
FDA Product Code
HIT FDA UDI
EMDN Code
Z1212012001 VISUAL FUNCTIONAL ASSESSMENT EQUIPMENT EUDAMED
GMDN Term
Binocular vision test unit FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
886.1170 FDA UDI
Market of Registration
Germany 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

C-Quant by OCULUS Optikgeräte GmbH — 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

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

Manufacturer

EUDAMED SRN
DE-MF-000012227

Sources (2)

  • EUDAMED 0e468bfe-8c1e-44c3-9155-8d091e67c7ce 61 fields · synced Jul 15, 2026
  • FDA UDI b216fd4b-8624-4daa-b507-0982f2458e04 34 fields · synced May 30, 2026