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Piccolo Composite Nailing System

FDA UDI

Class II (US FDA UDI)

by Carbofix Orthopedics Ltd

Identity

Trade Name
Piccolo Composite Nailing System FDA UDI
Generic Name
Bone awl, reusable FDA UDI
Device Name
Awl for use with the Piccolo Composite Tibia Nailing System. FDA UDI
Model / Reference
Awl FDA UDI
Description
Awl for use with the Piccolo Composite Tibia Nailing System. FDA UDI

Identifiers

Catalog Number
PFT910660 FDA UDI
Primary DI / UDI-DI
07290110200619 FDA UDI
510(k) Number
K102369 FDA UDI
K111056 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Bone awl, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Category: Bone awl, reusable

Piccolo Composite Nailing System by Carbofix Orthopedics Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Bone awl, reusable.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ac422f48-01c9-48e2-8a50-7364ec4b55c1 36 fields · synced May 31, 2026