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Legion

FDA UDI

Class II (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
LEGION FDA UDI
Generic Name
Bone-coring punch, single-use FDA UDI
Device Name
LEGION FASTPAK FIN PUNCH SIZE 5-6 FDA UDI
Model / Reference
71442241 FDA UDI
Description
LEGION FASTPAK FIN PUNCH SIZE 5-6 FDA UDI

Identifiers

Catalog Number
71442241 FDA UDI
Primary DI / UDI-DI
00885556648216 FDA UDI
FDA Product Code
JWH FDA UDI
LRY FDA UDI
GMDN Term
Bone-coring punch, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3560 FDA UDI
878.4800 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Bone-coring punch, single-use

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

Similar devices

Also classified as Bone-coring punch, 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 ae483ada-f3f5-4d83-a280-47072447ec1c 35 fields · synced Jun 8, 2026