Screw forceps, 45°, auto-fix

FDA UDI

Class I (US FDA UDI)

by United Orthopedic Corp.

Identity

Trade Name: Screw forceps, 45°, auto-fix FDA UDI
Generic Name: Implant handling forceps, scissors-like FDA UDI
Device Name: U2 Total Knee System FDA UDI
Model / Reference: 9601-1103-RA FDA UDI
Description: U2 Total Knee System FDA UDI

Identifiers

Catalog Number: 9601-1103-RA FDA UDI
Primary DI / UDI-DI: 04711605582513 FDA UDI
FDA Product Code: LXH FDA UDI
GMDN Term: Implant handling forceps, scissors-like 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

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

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Implant handling forceps, scissors-like

Screw forceps, 45°, auto-fix by United Orthopedic Corp. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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JAZZ System — Implanet · Class II

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: United Orthopedic Corp.

Sources (1)

FDA UDI 199b7d76-856a-45b9-9576-bc24045ab71a 35 fields · synced Jun 8, 2026