Quick Disconnect

FDA UDI

Class I (US FDA UDI)

by Curvafix Inc

Identity

Trade Name: Quick Disconnect FDA UDI
Generic Name: Surgical torque wrench adaptor FDA UDI
Device Name: An instrument that enables connection of the torque limiting handle to the Inserter during implantation of the CurvaFix IM Implant. FDA UDI
Model / Reference: PQD-001 FDA UDI
Description: An instrument that enables connection of the torque limiting handle to the Inserter during implantation of the CurvaFix IM Implant. FDA UDI

Identifiers

Catalog Number: PQD-001 FDA UDI
Primary DI / UDI-DI: 10855068008362 FDA UDI
FDA Product Code: LXH FDA UDI
HWC FDA UDI
HSB FDA UDI
GMDN Term: Surgical torque wrench adaptor FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.4540 FDA UDI
888.3040 FDA UDI
888.3020 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Surgical torque wrench adaptor

Quick Disconnect by Curvafix Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Curvafix Inc

Sources (1)

FDA UDI 0a4c79cd-a851-41e1-9771-f3e336fcadbc 35 fields · synced May 30, 2026