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Journey

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
JOURNEY FDA UDI
Generic Name
Total knee prosthesis implantation guide-instrument kit FDA UDI
Device Name
JOURNEY II CR FEMORAL FINISHING KIT LMR FDA UDI
Model / Reference
74010041KL FDA UDI
Description
JOURNEY II CR FEMORAL FINISHING KIT LMR FDA UDI

Identifiers

Catalog Number
74010041KL FDA UDI
Primary DI / UDI-DI
00885556295045 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Total knee prosthesis implantation guide-instrument kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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: Total knee prosthesis implantation guide-instrument kit

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

Similar devices

Also classified as Total knee prosthesis implantation guide-instrument kit.

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 d0c12b0b-6afe-4002-8c4e-caec0bfc0a8a 35 fields · synced Jun 8, 2026