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 3-4 FDA UDI
Model / Reference: 71442240 FDA UDI
Description: LEGION FASTPAK FIN PUNCH SIZE 3-4 FDA UDI

Identifiers

Catalog Number: 71442240 FDA UDI
Primary DI / UDI-DI: 00885556648209 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

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

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.

Single Use Professional — EAKIN SURGICAL LIMITED · Class I
PYRENEES® Cervical Plate System — K2M, INC. · Class I
OZARK Cervical Plate System — K2M, INC. · Class I
Single Use Professional — EAKIN SURGICAL LIMITED · Class I
Argo Knotless GENESYS — Conmed Corporation · Class I
Single Use Professional — EAKIN SURGICAL LIMITED · Class I
Single Use Professional — EAKIN SURGICAL LIMITED · Class I
Apollo — MEDLINE INDUSTRIES, INC. · Class I

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer: Smith & Nephew, Inc.

Sources (1)

FDA UDI cd113eb2-fac7-459d-b23e-1ab51f2e10ad 35 fields · synced Jun 8, 2026