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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
Surgical depth gauge, reusable FDA UDI
Device Name
Depth Gauge for use with the Piccolo Composite Proximal Femur Nailing System. FDA UDI
Model / Reference
K-Wire Depth Gauge FDA UDI
Description
Depth Gauge for use with the Piccolo Composite Proximal Femur Nailing System. FDA UDI

Identifiers

Catalog Number
PPF910290 FDA UDI
Primary DI / UDI-DI
07290109338057 FDA UDI
510(k) Number
K151010 FDA UDI
K153536 FDA UDI
FDA Product Code
HSB FDA UDI
GMDN Term
Surgical depth gauge, 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: Surgical depth gauge, 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 Surgical depth gauge, 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 401273e4-a122-4d87-b83a-da6618de1d4d 36 fields · synced May 30, 2026