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Procedure Product Torque Device

FDA UDI

Class II (US FDA UDI)

by Procedure Products, Inc.

Identity

Trade Name
Procedure Product Torque Device FDA UDI
Generic Name
Torque manipulation device FDA UDI
Device Name
TORQUE DEVICE, WHITE FDA UDI
Model / Reference
8014 FDA UDI
Description
TORQUE DEVICE, WHITE FDA UDI

Identifiers

Primary DI / UDI-DI
B16080141 FDA UDI
FDA Product Code
DQX FDA UDI
GMDN Term
Torque manipulation device FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
870.1330 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

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Torque manipulation device

Procedure Product Torque Device by Procedure Products, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Torque manipulation device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a00a4914-af97-4767-80dd-803b613d236e 33 fields · synced May 30, 2026