← Back to catalogue

Phantom® Fibula Nail System

FDA UDI

Class I (US FDA UDI)

by Paragon 28

Identity

Trade Name
Phantom® Fibula Nail System FDA UDI
Generic Name
Bone-resection orthopaedic reamer, single-use FDA UDI
Device Name
3.3mm Proximal Reamer, Cannulated, AO Quick Connect FDA UDI
Model / Reference
P36-925-3331 FDA UDI
Description
3.3mm Proximal Reamer, Cannulated, AO Quick Connect FDA UDI

Identifiers

Catalog Number
P36-925-3331 FDA UDI
Primary DI / UDI-DI
00889795146236 FDA UDI
FDA Product Code
HTO FDA UDI
GMDN Term
Bone-resection orthopaedic reamer, 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

Category: Bone-resection orthopaedic reamer, single-use

Phantom® Fibula Nail System by Paragon 28 — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone-resection orthopaedic reamer, single-use.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Paragon 28

Sources (1)

  • FDA UDI 0e21e478-b501-49fb-ab76-c0f5b5f95118 34 fields · synced May 30, 2026