Protract Hip HA System

FDA UDI

Class II (US FDA UDI)

by Globus Medical, Inc.

Identity

Trade Name: Protract Hip HA System FDA UDI
Generic Name: Coated hip femur prosthesis, modular FDA UDI
Device Name: Protract Press-Fit Hip Stem, Lateral, HA Coated FDA UDI
Model / Reference: SC2662-15 FDA UDI
Description: Protract Press-Fit Hip Stem, Lateral, HA Coated FDA UDI

Identifiers

Primary DI / UDI-DI: 10840843107569 FDA UDI
FDA Product Code: LPH FDA UDI
GMDN Term: Coated hip femur prosthesis, modular FDA UDI

Classification

Device Class: Class II FDA UDI
Regulation Number: 888.3358 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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

Yes

FDA UDI

Manufacturing Date

FDA UDI

Category: Coated hip femur prosthesis, modular

Protract Hip HA System by Globus Medical, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coated hip femur prosthesis, modular.

LCU Hip Stem — WALDEMAR LINK GmbH & Co. KG · Class II
ABG — Howmedica Osteonics Corp. · Class II
Z1™ Hip System — Zimmer, Inc. · Class II
DJO SURGICAL — ENCORE MEDICAL, L.P. · Class II
VerSys® — Zimmer, Inc. · Class II
CATALYSTEM — Smith & Nephew, Inc. · Class II
Everglade Stem, Standard Offset — SIGNATURE ORTHOPAEDICS PTY LTD · Class II
Excia® L — AESCULAP, INC. · 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 II	Pending data

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Manufacturer

Manufacturer: Globus Medical, Inc.

Sources (1)

FDA UDI b5a5ef39-613b-4570-9483-f2741ab48a5b 33 fields · synced Jun 1, 2026