Centronail Titanium Humeral Nailing System

FDA UDI

Class II (US FDA UDI)

by Orthofix, Inc.

Identity

Trade Name: Centronail Titanium Humeral Nailing System FDA UDI
Generic Name: Surgical countersink, single-use FDA UDI
Device Name: ANTEROGRADE CANNULATED REAMER FDA UDI
Model / Reference: 1 FDA UDI
Description: ANTEROGRADE CANNULATED REAMER FDA UDI

Identifiers

Catalog Number: 178261 FDA UDI
Primary DI / UDI-DI: 18032937168798 FDA UDI
FDA Product Code: JDS FDA UDI
GMDN Term: Surgical countersink, single-use 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

FDA UDI

Single Use

Yes

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Surgical countersink, single-use

Centronail Titanium Humeral Nailing System by Orthofix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class II	Pending data

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Manufacturer

Manufacturer: Orthofix, Inc.

Sources (1)

FDA UDI bd66a98f-2aa0-4ba3-8d57-d1a9e09d2806 35 fields · synced May 31, 2026