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Cannulated Headless Screw - Full Thread

FDA UDI

Class I (US FDA UDI)

by Tyber Medical

Identity

Trade Name
Cannulated Headless Screw - Full Thread FDA UDI
Generic Name
Surgical countersink, reusable FDA UDI
Device Name
CANN CNTRSNK F/2.0MM HEADED CANNULATED SCREW QC, REUSABLE FDA UDI
Model / Reference
03.333.923 FDA UDI
Description
CANN CNTRSNK F/2.0MM HEADED CANNULATED SCREW QC, REUSABLE FDA UDI

Identifiers

Primary DI / UDI-DI
00196449024667 FDA UDI
FDA Product Code
LXH FDA UDI
GMDN Term
Surgical countersink, reusable FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 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

Yes

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 countersink, reusable

Cannulated Headless Screw - Full Thread by Tyber Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Surgical countersink, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Tyber Medical

Sources (1)

  • FDA UDI e87840ce-c4c9-4dbb-92ab-9582ec413bf4 34 fields · synced Jun 8, 2026