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Journey

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
JOURNEY FDA UDI
Generic Name
Orthopaedic cement curette FDA UDI
Device Name
CEMENT SCRAPER FDA UDI
Model / Reference
74036159 FDA UDI
Description
CEMENT SCRAPER FDA UDI

Identifiers

Catalog Number
74036159 FDA UDI
Primary DI / UDI-DI
00885556703632 FDA UDI
FDA Product Code
HTF FDA UDI
GMDN Term
Orthopaedic cement curette 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

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: Orthopaedic cement curette

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

Similar devices

Also classified as Orthopaedic cement curette.

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 59a06ed8-0ec2-4e8a-b7f4-6d067c19f411 35 fields · synced Jun 8, 2026