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Alcon

FDA UDI

Class II (US FDA UDI)

by Alcon Laboratories, Inc.

Identity

Trade Name
Alcon FDA UDI
Generic Name
Fibreoptic operating light system FDA UDI
Device Name
Straight Pick Fiber Optic, Regular, 2.1m FDA UDI
Model / Reference
8065740260 FDA UDI
Description
Straight Pick Fiber Optic, Regular, 2.1m FDA UDI

Identifiers

Primary DI / UDI-DI
00380657402601 FDA UDI
FDA Product Code
HQE FDA UDI
GMDN Term
Fibreoptic operating light system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.4150 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Length — 2.1 Meter FDA UDI

Category: Fibreoptic operating light system

Alcon by Alcon Laboratories, 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

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Manufacturer

Manufacturer
Alcon Laboratories, Inc.

Sources (1)

  • FDA UDI 0d7b5c2e-ba8a-4189-bc26-11ed3453ea8d 35 fields · synced Jun 6, 2026