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Alcon

FDA UDI

Class II (US FDA UDI)

by Alcon Laboratories, Inc.

Identity

Trade Name
Alcon FDA UDI
Generic Name
Laser adaptor FDA UDI
Device Name
Zeiss/Moeller Dr. Filter FDA UDI
Model / Reference
8065750448 FDA UDI
Description
Zeiss/Moeller Dr. Filter FDA UDI

Identifiers

Primary DI / UDI-DI
00380657504480 FDA UDI
FDA Product Code
GEX FDA UDI
HQF FDA UDI
GMDN Term
Laser adaptor FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4810 FDA UDI
886.4390 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Laser adaptor

Alcon by Alcon Laboratories, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Laser adaptor.

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 86817171-45dd-4e2f-b268-a9d752130428 34 fields · synced May 30, 2026