Titan Reverse Shoulder System

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name: Titan Reverse Shoulder System FDA UDI
Generic Name: Orthopaedic reamer guide FDA UDI
Device Name: HUMERAL REAMER GUIDE BODY W/ DEFINITIVE STD MOD FDA UDI
Model / Reference: DGB-0960-08STD FDA UDI
Description: HUMERAL REAMER GUIDE BODY W/ DEFINITIVE STD MOD FDA UDI

Identifiers

Catalog Number: DGB-0960-08STD FDA UDI
Primary DI / UDI-DI: 00885556863626 FDA UDI
FDA Product Code: LXH FDA UDI
GMDN Term: Orthopaedic reamer guide 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 reamer guide

Titan Reverse Shoulder System by Smith & Nephew, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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MAXIM EM TIBIAL GUIDE — Biomet Orthopedics, Inc. · Class I

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: Smith & Nephew, Inc.

Sources (1)

FDA UDI fa8a09b3-9157-4df3-ad5b-42f2c7dc02cd 35 fields · synced Jun 8, 2026