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Orascoptic - OmniOpti HDL 2.5

FDA UDI

Class I (US FDA UDI)

by Metrex Research

Identity

Trade Name
Orascoptic - OmniOpti HDL 2.5 FDA UDI
Generic Name
Surgical binoculars, reusable FDA UDI
Device Name
OmniOptic™ Ocular Pair - HDL™ 2.5, Plano FDA UDI
Model / Reference
OmniOpti HDL 2.5 FDA UDI
Description
OmniOptic™ Ocular Pair - HDL™ 2.5, Plano FDA UDI

Identifiers

Primary DI / UDI-DI
10615375009595 FDA UDI
FDA Product Code
FSP FDA UDI
GMDN Term
Surgical binoculars, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

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

Category: Surgical binoculars, reusable

Orascoptic - OmniOpti HDL 2.5 by Metrex Research — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical binoculars, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Metrex Research

Sources (1)

  • FDA UDI dd0f24ff-0486-4d1c-827c-1d1bd2f8f58f 35 fields · synced May 30, 2026