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Suture Fisher Hip

FDA UDI

Class I (US FDA UDI)

by Gm Dos Reis Industria E Comercio Ltda

Identity

Trade Name
Suture Fisher Hip FDA UDI
Generic Name
Suturing unit, single-use FDA UDI
Device Name
Suture Fisher Hip - Suture Holder 45° to the Right FDA UDI
Model / Reference
Suture Holder 45° to the Right FDA UDI
Description
Suture Fisher Hip - Suture Holder 45° to the Right FDA UDI

Identifiers

Catalog Number
361-50 FDA UDI
Primary DI / UDI-DI
07899258662619 FDA UDI
FDA Product Code
HWQ FDA UDI
GMDN Term
Suturing unit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Suturing unit, single-use

Suture Fisher Hip by Gm Dos Reis Industria E Comercio Ltda — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Suturing unit, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2df5ef40-5121-4087-b71d-422ef15ae274 34 fields · synced May 30, 2026