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Razek Equipamentos

FDA UDI

Class I (US FDA UDI)

by Razek Equipamentos Ltda

Identity

Trade Name
RAZEK EQUIPAMENTOS FDA UDI
Generic Name
Suturing unit, single-use FDA UDI
Device Name
Razek Suture Passer Hook - FitPass FDA UDI
Model / Reference
742640000 FDA UDI
Description
Razek Suture Passer Hook - FitPass FDA UDI

Identifiers

Primary DI / UDI-DI
07898994583462 FDA UDI
FDA Product Code
NBH FDA UDI
GMDN Term
Suturing unit, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.1100 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

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

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Suturing unit, single-use

Razek Equipamentos by Razek Equipamentos 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 9a577cb5-43ef-4f78-a4d6-7a4c15d827fc 33 fields · synced May 30, 2026