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Trigen

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
TRIGEN FDA UDI
Generic Name
Orthopaedic guidewire, single-use FDA UDI
Device Name
3.0MM X 900MM BALL TIP GUIDE ROD FDA UDI
Model / Reference
71118202 FDA UDI
Description
3.0MM X 900MM BALL TIP GUIDE ROD FDA UDI

Identifiers

Catalog Number
71118202 FDA UDI
Primary DI / UDI-DI
03596010298348 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Orthopaedic guidewire, single-use 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

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

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Orthopaedic guidewire, single-use

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

Similar devices

Also classified as Orthopaedic guidewire, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI a0eaaeab-e10d-43b7-b529-6ceb59ad0b69 35 fields · synced Jun 8, 2026