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Centronail Titanium Supracondylar Nailing System

FDA UDI

Class II (US FDA UDI)

by Orthofix, Inc.

Identity

Trade Name
Centronail Titanium Supracondylar Nailing System FDA UDI
Generic Name
Orthopaedic bone screw, non-bioabsorbable, sterile FDA UDI
Device Name
TITANIUM CONDYLAR LOCKING SCREW D.4.8 MM-L.75 MM FDA UDI
Model / Reference
1 FDA UDI
Description
TITANIUM CONDYLAR LOCKING SCREW D.4.8 MM-L.75 MM FDA UDI

Identifiers

Catalog Number
99-T766075 FDA UDI
Primary DI / UDI-DI
18032937161607 FDA UDI
FDA Product Code
JDS FDA UDI
HSB FDA UDI
GMDN Term
Orthopaedic bone screw, non-bioabsorbable, sterile FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3030 FDA UDI
888.3020 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

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

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 75 Millimeter FDA UDI
Outer Diameter — 4.8 Millimeter FDA UDI

Category: Orthopaedic bone screw, non-bioabsorbable, sterile

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

Similar devices

Also classified as Orthopaedic bone screw, non-bioabsorbable, sterile.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Orthofix, Inc.

Sources (1)

  • FDA UDI cf296822-67f4-4a11-95ff-64939c46e893 36 fields · synced May 31, 2026