Bristow Latarjet

FDA UDI

Class I (US FDA UDI)

by DePuy Mitek, Inc.

Identity

Trade Name: BRISTOW LATARJET FDA UDI
Generic Name: Orthopaedic instrument surgical connector FDA UDI
Device Name: Bristow - Latarjet Instability Shoulder System Coracoid 3.5mm Screw FDA UDI
Model / Reference: 285255 FDA UDI
Description: Bristow - Latarjet Instability Shoulder System Coracoid 3.5mm Screw FDA UDI

Identifiers

Catalog Number: 285255 FDA UDI
Primary DI / UDI-DI: 10886705017973 FDA UDI
FDA Product Code: LXH FDA UDI
GMDN Term: Orthopaedic instrument surgical connector 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

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Orthopaedic instrument surgical connector

Bristow Latarjet by DePuy Mitek, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Solstice Occipito-Cervico-Thoracic System — Life Spine, Inc. · Class II
DJO SURGICAL — ENCORE MEDICAL, L.P. · Class I
Pilot Spinal System — Life Spine, Inc. · Class II
MIS Curved Rod, Ø5.5 x 85mm — Captiva Spine · 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: DePuy Mitek, Inc.

Sources (1)

FDA UDI e720a1c6-0ff0-47df-85c9-99a8a82ba143 36 fields · synced May 30, 2026