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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
Razek PLM Instruments - Posterior Simple Calcaneus Plate Guide 05-D FDA UDI
Model / Reference
490061390 FDA UDI
Description
Razek PLM Instruments - Posterior Simple Calcaneus Plate Guide 05-D FDA UDI

Identifiers

Primary DI / UDI-DI
07908882884592 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic surgical procedure kit, non-medicated, reusable 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

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 94000621-7b79-490e-b74c-0a64815b8f35 33 fields · synced Jun 6, 2026