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Bionnovation

FDA UDI

Class I (US FDA UDI)

by Bionnovation Produtos Biomedicos Ltda.

Identity

Trade Name
BIONNOVATION FDA UDI
Generic Name
Surgical torque wrench, reusable FDA UDI
Device Name
DRIVE LOCK FOR RATCHET BIODIRECT SHORT FDA UDI
Model / Reference
13051 FDA UDI
Description
DRIVE LOCK FOR RATCHET BIODIRECT SHORT FDA UDI

Identifiers

Catalog Number
13051 FDA UDI
Primary DI / UDI-DI
07899943600735 FDA UDI
FDA Product Code
DZN FDA UDI
GMDN Term
Surgical torque wrench, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
872.4565 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

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
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical torque wrench, reusable

Bionnovation by Bionnovation Produtos Biomedicos Ltda. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical torque wrench, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 535954c0-e7ec-4fdf-bef0-6de66affe27f 34 fields · synced May 30, 2026