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Titan Modular Shoulder System

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
Titan Modular Shoulder System FDA UDI
Generic Name
Humeral body prosthesis trial FDA UDI
Device Name
BODY TRIAL 8 STANDARD FDA UDI
Model / Reference
TRL-0920-020-08STD FDA UDI
Description
BODY TRIAL 8 STANDARD FDA UDI

Identifiers

Catalog Number
T92002008STD FDA UDI
Primary DI / UDI-DI
00885556862674 FDA UDI
FDA Product Code
HWT FDA UDI
GMDN Term
Humeral body prosthesis trial FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Humeral body prosthesis trial

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

Similar devices

Also classified as Humeral body prosthesis trial.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 7bcb6fad-e05e-4ff3-93b8-4b64b7062af0 35 fields · synced Jun 8, 2026