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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
Orthopaedic surgical procedure kit, non-medicated, reusable FDA UDI
Device Name
Love, Upwards Cutting, 3,4 mm bite width, 350 mm (R068) FDA UDI
Model / Reference
742461700 FDA UDI
Description
Love, Upwards Cutting, 3,4 mm bite width, 350 mm (R068) FDA UDI

Identifiers

Primary DI / UDI-DI
07908882881379 FDA UDI
FDA Product Code
NBH FDA UDI
GMDN Term
Orthopaedic surgical procedure kit, non-medicated, reusable 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

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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic surgical procedure kit, non-medicated, reusable

Razek Equipamentos by Razek Equipamentos Ltda — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic surgical procedure kit, non-medicated, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Razek Equipamentos Ltda

Sources (1)

  • FDA UDI f4c29e85-5c1d-48f8-b346-8d7cfeb56d5e 33 fields · synced May 31, 2026