SOLID HEX DRIVER 2.5mm

FDA UDI

Class I (US FDA UDI)

by Advanced Orthopaedic Solutions, Inc.

Identity

Trade Name: SOLID HEX DRIVER 2.5mm FDA UDI
Generic Name: Surgical screwdriver, single-use, non-sterile FDA UDI
Model / Reference: 5006 FDA UDI

Identifiers

Primary DI / UDI-DI: 00848665019049 FDA UDI
FDA Product Code: LXH FDA UDI
GMDN Term: Surgical screwdriver, single-use, non-sterile 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

Yes

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

Yes

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Surgical screwdriver, single-use, non-sterile

A comprehensive medical device directory entry for the SOLID HEX DRIVER 2.5mm surgical screwdriver.

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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: Advanced Orthopaedic Solutions, Inc.

Sources (1)

FDA UDI a744a8c0-a08d-44c5-8f43-e3ae74cdbd84 33 fields · synced Jul 11, 2026