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Titan Modular Shoulder System 2.5

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
Titan Modular Shoulder System 2.5 FDA UDI
Generic Name
Orthopaedic implant/instrument assembling device FDA UDI
Device Name
TRIAL OSTEOTOMY COVER -S FDA UDI
Model / Reference
CVR-0920-076S FDA UDI
Description
TRIAL OSTEOTOMY COVER -S FDA UDI

Identifiers

Catalog Number
CVR-0920-076S FDA UDI
Primary DI / UDI-DI
00885556860014 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic implant/instrument assembling device 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

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: Orthopaedic implant/instrument assembling device

Titan Modular Shoulder System 2.5 by Smith & Nephew, Inc. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic implant/instrument assembling device.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Smith & Nephew, Inc.

Sources (1)

  • FDA UDI 84efcdd8-9997-4568-8100-cddd187b12bb 35 fields · synced Jun 8, 2026