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Bun-Yo-Matic™ Lapidus Clamp System

FDA UDI

Class I (US FDA UDI)

by Paragon 28

Identity

Trade Name
Bun-Yo-Matic™ Lapidus Clamp System FDA UDI
Generic Name
Orthopaedic guidewire, single-use FDA UDI
Device Name
K-Wire, Olive, Threaded, Ø1.8mm x 4.7cm FDA UDI
Model / Reference
P99-251-1604 FDA UDI
Description
K-Wire, Olive, Threaded, Ø1.8mm x 4.7cm FDA UDI

Identifiers

Catalog Number
P99-251-1604 FDA UDI
Primary DI / UDI-DI
00889795131386 FDA UDI
FDA Product Code
HXI 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

No

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
MRI Safety
MR Unsafe FDA UDI

Category: Orthopaedic guidewire, single-use

Bun-Yo-Matic™ Lapidus Clamp System by Paragon 28 — 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

Manufacturer
Paragon 28

Sources (1)

  • FDA UDI 0075e508-9714-4420-b009-e5825c40a106 34 fields · synced May 30, 2026