Journey Ii Fastpak

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name: JOURNEY II FASTPAK FDA UDI
Generic Name: Knee tibia prosthesis trial, single-use FDA UDI
Device Name: JOURNEY II FASTPAK SIZE 3-4 RIGHT INSERT TRIALS AND SPACERS 9-13,15 MM FDA UDI
Model / Reference: 74012034 FDA UDI
Description: JOURNEY II FASTPAK SIZE 3-4 RIGHT INSERT TRIALS AND SPACERS 9-13,15 MM FDA UDI

Identifiers

Catalog Number: 74012034 FDA UDI
Primary DI / UDI-DI: 00885556808399 FDA UDI
FDA Product Code: HWT FDA UDI
GMDN Term: Knee tibia prosthesis trial, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 888.4800 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

Yes

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Knee tibia prosthesis trial, single-use

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

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Also classified as Knee tibia prosthesis trial, single-use.

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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 I	Pending data

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Manufacturer

Manufacturer: Smith & Nephew, Inc.

Sources (1)

FDA UDI c1b66b8c-1af3-473e-9241-bd0e667048f1 35 fields · synced Jun 8, 2026