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Clement Clarke Ophthalmic

FDA UDI

Class II (US FDA UDI)

by Haag-Streit Uk Limited

Identity

Trade Name
Clement Clarke Ophthalmic FDA UDI
Generic Name
Ophthalmic examination slit lamp FDA UDI
Device Name
BA904 SLIT LAMP SET C (05) FDA UDI
Model / Reference
5606013 US FDA UDI
Description
BA904 SLIT LAMP SET C (05) FDA UDI

Identifiers

Catalog Number
5606013 US FDA UDI
Primary DI / UDI-DI
05060179470313 FDA UDI
510(k) Number
K953965 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

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Ophthalmic examination slit lamp

Clement Clarke Ophthalmic by Haag-Streit Uk Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Ophthalmic examination slit lamp.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 49f129b0-0af3-4592-9388-4db37bed0b86 36 fields · synced May 30, 2026