1.5 / 2.0 / 3.0 Trauma Screw Tray Instruments

FDA UDI

Class I (US FDA UDI)

by Tyber Medical

Identity

Trade Name: 1.5 / 2.0 / 3.0 Trauma Screw Tray Instruments FDA UDI
Generic Name: Cannulated surgical drill bit, single-use FDA UDI
Device Name: Ø2.0 (6") Drill FDA UDI
Model / Reference: 001-120116 FDA UDI
Description: Ø2.0 (6") Drill FDA UDI

Identifiers

Catalog Number: 001-120116 FDA UDI
Primary DI / UDI-DI: M6950011201160 FDA UDI
FDA Product Code: LXH FDA UDI
GMDN Term: Cannulated surgical drill bit, single-use 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

FDA UDI

Single Use

FDA UDI

Implantable

FDA UDI

Contains Latex

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

FDA UDI

Convenience Kit

FDA UDI

Combination Product

FDA UDI

HCT/P

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Cannulated surgical drill bit, single-use

1.5 / 2.0 / 3.0 Trauma Screw Tray Instruments by Tyber Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Source	Region	Type	Cert / Approval No.	Class	Status
FDA UDI	United States	FDA UDI	Registered in GUDID	Class I	Pending data

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Manufacturer

Manufacturer: Tyber Medical

Sources (1)

FDA UDI bbd50cfb-44e3-4c90-8026-336a8af47343 35 fields · synced May 31, 2026