← Back to catalogue

Lucent

FDA UDI

Class II (US FDA UDI)

by Spinal Elements, Inc.

Identity

Trade Name
LUCENT FDA UDI
Generic Name
Fibreoptic operating light system FDA UDI
Device Name
Bifurcated Fiber Optic Clip On Cable, Angled FDA UDI
Model / Reference
81101-002 FDA UDI
Description
Bifurcated Fiber Optic Clip On Cable, Angled FDA UDI

Identifiers

Primary DI / UDI-DI
00840606114943 FDA UDI
FDA Product Code
FST FDA UDI
GMDN Term
Fibreoptic operating light system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4580 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

No

FDA UDI

Lot / Batch Number

Yes

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: Fibreoptic operating light system

Lucent by Spinal Elements, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Fibreoptic operating light system.

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
Spinal Elements, Inc.

Sources (1)

  • FDA UDI 64a4583d-a2f3-43b1-b941-eff7fa0a1812 33 fields · synced May 30, 2026