← Back to catalogue

OACF-17 Three Mirror 17mm Lens Flange Adapter

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 8953

by Ocular Instruments Inc.

Identity

Trade Name
OACF-17 Three Mirror 17mm Lens Flange Adapter EUDAMED
Three Mirror 17mm Lens Flange Adapter FDA UDI
Generic Name
Gonioscope FDA UDI
Device Name
Contact Ophthalmic EUDAMED
Model / Reference
8953 EUDAMED
OACF-17 FDA UDI

Identifiers

Primary DI / UDI-DI
00630238089531 EUDAMEDFDA UDI
Basic UDI-DI
06302381262637 EUDAMED
Direct Marketing DI
00630238089555 EUDAMED
FDA Product Code
HKS FDA UDI
EMDN Code
Q0299 OPHTHALMIC DEVICES - OTHER EUDAMED
GMDN Term
Gonioscope FDA UDI

Classification

Device Class
Class I EUDAMEDFDA UDI
Regulation Number
886.1660 FDA UDI
Market of Registration
Austria 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

OACF-17 Three Mirror 17mm Lens Flange Adapter by Ocular Instruments, 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

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

Manufacturer

EUDAMED SRN
US-MF-000007216
Authorised Representative
Emergo Europe B.V. NL-AR-000000116

Sources (2)

  • EUDAMED 8fe9514e-ad97-4bdd-98f3-c842495ac3b8 61 fields · synced Jun 18, 2026
  • FDA UDI b7731446-6b5d-4946-8493-4e2c807cf786 32 fields · synced May 30, 2026