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Binoptometer 4P

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 59862

by OCULUS Optikgeräte GmbH

Identity

Trade Name
Binoptometer 4P EUDAMEDFDA UDI
Generic Name
Binocular vision test unit FDA UDI
Device Name
Binoptometer EUDAMED
Binoptometer 4P FDA UDI
Model / Reference
59862 EUDAMEDFDA UDI
Description
Binoptometer 4P FDA UDI

Identifiers

Primary DI / UDI-DI
04049584010049 EUDAMEDFDA UDI
Basic UDI-DI
404958410PL EUDAMED
FDA Product Code
HJQ FDA UDI
HOX 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
886.1870 FDA UDI
886.1150 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

Binoptometer 4P 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

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Manufacturer

EUDAMED SRN
DE-MF-000012227

Sources (2)

  • EUDAMED e0e7bebf-ef3b-4b04-87a4-1db8588ee094 61 fields · synced Aug 2, 2026
  • FDA UDI 81def42b-233b-48c6-b5d0-3bc6556ffa08 34 fields · synced May 26, 2026