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Headed Screw System Instruments

FDA UDI

Class I (US FDA UDI)

by Tyber Medical

Identity

Trade Name
Headed Screw System Instruments FDA UDI
Generic Name
Surgical countersink, reusable FDA UDI
Device Name
5.0 / 5.5 Screw Countersink FDA UDI
Model / Reference
009-000045 FDA UDI
Description
5.0 / 5.5 Screw Countersink FDA UDI

Identifiers

Catalog Number
009-000045 FDA UDI
Primary DI / UDI-DI
M6950090000450 FDA UDI
FDA Product Code
HWW 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

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

Category: Surgical countersink, reusable

Headed Screw System Instruments 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 d6e6d180-b4a1-415f-830c-1c90779fa61e 35 fields · synced Jun 1, 2026