← Back to catalogue

Orion Headed Screw

FDA UDI

Class II (US FDA UDI)

by Tyber Medical

Identity

Trade Name
Orion Headed Screw FDA UDI
Generic Name
Orthopaedic bone screw (non-sliding) FDA UDI
Device Name
Headed Cannulated Screw Short-Thread Ø2.5mm-(L) 12mm FDA UDI
Model / Reference
HTR-04-254112 FDA UDI
Description
Headed Cannulated Screw Short-Thread Ø2.5mm-(L) 12mm FDA UDI

Identifiers

Catalog Number
HTR-04-254112 FDA UDI
Primary DI / UDI-DI
M695HTR042541120 FDA UDI
FDA Product Code
HWC FDA UDI
GMDN Term
Orthopaedic bone screw (non-sliding) FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Commercial Distribution
Not in Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI
MRI Safety
MR Conditional FDA UDI

Orion Headed Screw by Tyber Medical — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Tyber Medical

Sources (1)

  • FDA UDI 445f3550-43ed-4061-abac-b60bc4640f91 36 fields · synced May 31, 2026