← Back to catalogue

Clement Clarke Ophthalmic

FDA UDI

Class I (US FDA UDI)

by Haag-Streit Uk Limited

Identity

Trade Name
Clement Clarke Ophthalmic FDA UDI
Generic Name
Maddox wing FDA UDI
Device Name
MADDOX WING TEST FDA UDI
Model / Reference
7005001 FDA UDI
Description
MADDOX WING TEST FDA UDI

Identifiers

Catalog Number
7005001 FDA UDI
Primary DI / UDI-DI
05060179470399 FDA UDI
FDA Product Code
HKW FDA UDI
GMDN Term
Maddox wing FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
886.1650 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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Maddox wing

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

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

Sources (1)

  • FDA UDI fd4a6bea-3094-4797-9fa9-fcc0f7eef951 35 fields · synced May 30, 2026