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Panta 2 Arthrodesis Nail System

FDA UDI

Class I (US FDA UDI)

by Smith & Nephew, Inc.

Identity

Trade Name
Panta 2 Arthrodesis Nail System FDA UDI
Generic Name
Orthopaedic guidewire, single-use FDA UDI
Device Name
GUIDE WIRE. 3.2MM DIAMETER X 600MM FDA UDI
Model / Reference
PAN-1010-0034 FDA UDI
Description
GUIDE WIRE. 3.2MM DIAMETER X 600MM FDA UDI

Identifiers

Catalog Number
PAN-1010-0034 FDA UDI
Primary DI / UDI-DI
00885556828694 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

Panta 2 Arthrodesis Nail System 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 b0a05c88-a7bf-4c2a-941e-b3bb7fe639dc 35 fields · synced Jun 8, 2026