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General Instrument

FDA UDI

Class I (US FDA UDI)

by Limacorporate

Identity

Trade Name
General Instrument FDA UDI
Generic Name
Surgical torque wrench, reusable FDA UDI
Device Name
General Instrument - Torque Wrench AO Connection 2.5Nm FDA UDI
Model / Reference
9095.11.754 FDA UDI
Description
General Instrument - Torque Wrench AO Connection 2.5Nm FDA UDI

Identifiers

Catalog Number
9095.11.754 FDA UDI
Primary DI / UDI-DI
08033390301879 FDA UDI
FDA Product Code
HRW FDA UDI
GMDN Term
Surgical torque wrench, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.1250 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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Surgical torque wrench, reusable

General Instrument by Limacorporate — 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

Manufacturer
Limacorporate

Sources (1)

  • FDA UDI b7842182-4eb4-4f8d-8444-8d9c1d2d7e4b 34 fields · synced Jun 1, 2026