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HA Bone Screws

FDA UDI

Class II (US FDA UDI)

by Orthofix, Inc.

Identity

Trade Name
HA Bone Screws FDA UDI
Generic Name
Orthopaedic bone pin, non-bioabsorbable FDA UDI
Device Name
OSTEOTITE BONE SCREW 80/30 MM SHAFT D 6MM THREAD D 4.5-3.5MM FDA UDI
Model / Reference
1 FDA UDI
Description
OSTEOTITE BONE SCREW 80/30 MM SHAFT D 6MM THREAD D 4.5-3.5MM FDA UDI

Identifiers

Catalog Number
SS99-60108 FDA UDI
Primary DI / UDI-DI
18032568867626 FDA UDI
FDA Product Code
JDW FDA UDI
GMDN Term
Orthopaedic bone pin, non-bioabsorbable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

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
Outer Diameter — 6 Millimeter FDA UDI
Length — 80 Millimeter FDA UDI

Category: Orthopaedic bone pin, non-bioabsorbable

HA Bone Screws by Orthofix, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic bone pin, non-bioabsorbable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Orthofix, Inc.

Sources (1)

  • FDA UDI 15d97e56-46b6-4090-b918-963995e8d8b0 36 fields · synced May 30, 2026