← Back to catalogue

Haag Streit John Weiss

FDA UDI

Class I (US FDA UDI)

by Haag-Streit Uk Limited

Identity

Trade Name
Haag Streit John Weiss FDA UDI
Generic Name
Periocular/lacrimal retractor, hand-held, reusable FDA UDI
Device Name
RETRACTOR WATSON ORBITAL SGL BLD FDA UDI
Model / Reference
0107073 FDA UDI
Description
RETRACTOR WATSON ORBITAL SGL BLD FDA UDI

Identifiers

Catalog Number
0107073 FDA UDI
Primary DI / UDI-DI
05055296017497 FDA UDI
FDA Product Code
MDM FDA UDI
GMDN Term
Periocular/lacrimal retractor, hand-held, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Periocular/lacrimal retractor, hand-held, reusable

Haag Streit John Weiss by Haag-Streit Uk Limited — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Periocular/lacrimal retractor, hand-held, reusable.

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

Manufacturer
Haag-Streit Uk Limited

Sources (1)

  • FDA UDI 57774b58-fb75-4f1f-9e04-4982898db6d5 35 fields · synced May 30, 2026