← Back to catalogue

Fiber Optic Light Wand

FDA UDI

Class I (US FDA UDI)

by Flexbar Machine Corp.

Identity

Trade Name
Fiber Optic Light Wand FDA UDI
Generic Name
Operating room light FDA UDI
Device Name
Flex-Light Fiber Optic Light Clip (for Mini-Bookler Systems) FDA UDI
Model / Reference
72077-Mini FDA UDI
Description
Flex-Light Fiber Optic Light Clip (for Mini-Bookler Systems) FDA UDI

Identifiers

Primary DI / UDI-DI
00842102111815 FDA UDI
FDA Product Code
FDG FDA UDI
GMDN Term
Operating room light FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
876.4530 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

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Operating room light

Fiber Optic Light Wand by Flexbar Machine Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Operating room light.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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

Manufacturer

Manufacturer
Flexbar Machine Corp.

Sources (1)

  • FDA UDI 8049e0c9-e2fd-4392-9edd-a9ba9c86b1b0 33 fields · synced May 29, 2026