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Centerfield 2

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 56980

by OCULUS Optikgeräte GmbH

Identity

Trade Name
Centerfield 2 EUDAMEDFDA UDI
Generic Name
Perimeter, automatic FDA UDI
Device Name
Centerfield EUDAMED
Centerfield 2 FDA UDI
Model / Reference
56980 EUDAMEDFDA UDI
Description
Centerfield 2 FDA UDI

Identifiers

Primary DI / UDI-DI
04049584000125 EUDAMEDFDA UDI
Basic UDI-DI
404958426Q3 EUDAMED
FDA Product Code
HPT FDA UDI
HOO FDA UDI
EMDN Code
Z1212012003 PERIPHERAL VISION ANALYSERS EUDAMED
GMDN Term
Perimeter, automatic FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
886.1605 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

Centerfield 2 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 ab7c67f8-ab42-4fe5-9bf1-32f6627132f7 61 fields · synced Aug 1, 2026
  • FDA UDI 245c5e4b-0204-46cd-91a1-fe5f4af272d2 34 fields · synced May 30, 2026