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Universal Flip - Rx

FDA UDI

Class I (US FDA UDI)

by Metrex Research

Identity

Trade Name
Universal Flip - Rx FDA UDI
Generic Name
Surgical binoculars, reusable FDA UDI
Device Name
Universal Flip loupe with prescription lenses FDA UDI
Model / Reference
.UNIVERSAL.FLIP.TITAN.ONE-SIZE.* FDA UDI
Description
Universal Flip loupe with prescription lenses FDA UDI

Identifiers

Primary DI / UDI-DI
00615375010136 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

Universal Flip - Rx 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 fb2812f8-e391-45d3-a620-c4f18d4f7514 35 fields · synced Jun 6, 2026