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OLSLT Latina SLT Gonio Laser Lens

EUDAMEDFDA UDI

Class I (EU MDR)

Ref 7432

by Ocular Instruments Inc.

Identity

Trade Name
OLSLT Latina SLT Gonio Laser Lens EUDAMED
Latina SLT Gonio Laser Lens FDA UDI
Generic Name
Gonioscope FDA UDI
Device Name
Contact Ophthalmic EUDAMED
Model / Reference
7432 EUDAMED
OLSLT FDA UDI

Identifiers

Primary DI / UDI-DI
00630238074322 EUDAMEDFDA UDI
Basic UDI-DI
06302381262637 EUDAMED
Direct Marketing DI
00630238074346 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
High-level Disinfectant FDA UDI

OLSLT Latina SLT Gonio Laser Lens 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

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Manufacturer

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

Sources (2)

  • EUDAMED 907d919b-4611-45fc-9dd7-5f718c17b6c7 61 fields · synced Jul 16, 2026
  • FDA UDI fd952104-0ce2-4e01-887e-842b4a0101c6 32 fields · synced May 30, 2026