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Legion Revision

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
LEGION REVISION FDA UDI
Generic Name
Knee tibia prosthesis trial, reusable FDA UDI
Device Name
STEMLESS REVISION TIBIA TRIAL SZ 2 RT FDA UDI
Model / Reference
E0017190-8 FDA UDI
Description
STEMLESS REVISION TIBIA TRIAL SZ 2 RT FDA UDI

Identifiers

Catalog Number
E0017190-8 FDA UDI
Primary DI / UDI-DI
00885556798317 FDA UDI
FDA Product Code
HRY FDA UDI
GMDN Term
Knee tibia prosthesis trial, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3530 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: Knee tibia prosthesis trial, reusable

Legion Revision by Smith & Nephew, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Knee tibia prosthesis trial, reusable.

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 db8aae24-6d08-4614-9cb9-ca2b1d3b8d21 35 fields · synced Jun 8, 2026