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Precision MIS Bunion System

FDA UDI

Class I (US FDA UDI)

by Paragon 28

Identity

Trade Name
Precision MIS Bunion System FDA UDI
Generic Name
Orthopaedic guidewire, single-use FDA UDI
Device Name
Ø1.2 x 230mm Smooth K-wire for Ø3.0 Screw FDA UDI
Model / Reference
P27-192-3023 FDA UDI
Description
Ø1.2 x 230mm Smooth K-wire for Ø3.0 Screw FDA UDI

Identifiers

Catalog Number
P27-192-3023 FDA UDI
Primary DI / UDI-DI
00889795153326 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 Conditional FDA UDI

Category: Orthopaedic guidewire, single-use

Precision MIS Bunion 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 0275ea9f-9fc8-47f7-9896-df092f5c9224 34 fields · synced May 31, 2026