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Legion

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
LEGION FDA UDI
Generic Name
External orthopaedic fixation system, single-use FDA UDI
Device Name
LEGION CR & PS DCF FEMORAL INSTRUMENT KIT 3 OF 4 FDA UDI
Model / Reference
71441506KT FDA UDI
Description
LEGION CR & PS DCF FEMORAL INSTRUMENT KIT 3 OF 4 FDA UDI

Identifiers

Catalog Number
71441506KT FDA UDI
Primary DI / UDI-DI
00885556158494 FDA UDI
FDA Product Code
FSM FDA UDI
GMDN Term
External orthopaedic fixation system, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

Yes

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: External orthopaedic fixation system, single-use

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

Similar devices

Also classified as External orthopaedic fixation system, single-use.

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 fb517a38-32a7-45c6-aab3-c9e498f1f5ce 35 fields · synced Jun 8, 2026