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Piccolo Composite Plate System

FDA UDI

Class II (US FDA UDI)

by Carbofix Orthopedics Ltd

Identity

Trade Name
Piccolo Composite Plate System FDA UDI
Generic Name
Orthopaedic trocar blade, reusable FDA UDI
Device Name
Trocar for use with the Piccolo Composite Distal Femur Plate System FDA UDI
Model / Reference
Trocar FDA UDI
Description
Trocar for use with the Piccolo Composite Distal Femur Plate System FDA UDI

Identifiers

Catalog Number
DF930050 FDA UDI
Primary DI / UDI-DI
07290109337616 FDA UDI
510(k) Number
K143496 FDA UDI
FDA Product Code
KTT FDA UDI
HRS FDA UDI
GMDN Term
Orthopaedic trocar blade, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 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

Dimensions & Sizes

Size
Outer Diameter — 4.3 Millimeter FDA UDI

Category: Orthopaedic trocar blade, reusable

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

Similar devices

Also classified as Orthopaedic trocar blade, 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 186bc9f9-49a7-4252-9169-8b37532ab430 37 fields · synced May 30, 2026