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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
Orthopaedic implant aiming arm FDA UDI
Device Name
An instrument for use with the Piccolo Composite Humeral Nailing Systems Handle. FDA UDI
Model / Reference
Inner Rod FDA UDI
Description
An instrument for use with the Piccolo Composite Humeral Nailing Systems Handle. FDA UDI

Identifiers

Catalog Number
Q9105850 FDA UDI
Primary DI / UDI-DI
07290109339603 FDA UDI
510(k) Number
K091425 FDA UDI
K100497 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Orthopaedic implant aiming arm 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: Orthopaedic implant aiming arm

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 Orthopaedic implant aiming arm.

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 d392e9ba-8417-4cb9-9abd-7db0c4586193 36 fields · synced Jun 8, 2026