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Alcon

FDA UDI

Class II (US FDA UDI)

by Costruzioni Strumenti Oftalmici C.s.o. Srl

Identity

Trade Name
ALCON FDA UDI
Generic Name
Ophthalmic examination slit lamp FDA UDI
Device Name
SLIT LAMP SL 1000 REF 542-1255-001 FDA UDI
Model / Reference
SLIT LAMP SL 1000 FDA UDI
Description
SLIT LAMP SL 1000 REF 542-1255-001 FDA UDI

Identifiers

Catalog Number
100209A50 FDA UDI
Primary DI / UDI-DI
08056098470029 FDA UDI
FDA Product Code
HJO FDA UDI
GMDN Term
Ophthalmic examination slit lamp FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
886.1850 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

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: Ophthalmic examination slit lamp

Alcon by Costruzioni Strumenti Oftalmici C.s.o. Srl — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic examination slit lamp.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 4efb1156-61a3-4151-a6ec-dc73b4645a64 34 fields · synced Jun 6, 2026