CrossDrive

FDA UDI

Class I (US FDA UDI)

by Karl Storz GmbH & Co. KG

Identity

Trade Name: CrossDrive FDA UDI
Generic Name: Surgical screwdriver, reusable FDA UDI
Device Name: CrossDrive Plus Screwdriver FDA UDI
Model / Reference: 28789CD FDA UDI
Description: CrossDrive Plus Screwdriver FDA UDI

Identifiers

Primary DI / UDI-DI: 04048551115268 FDA UDI
FDA Product Code: LXH FDA UDI
GMDN Term: Surgical screwdriver, 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

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: Surgical screwdriver, reusable

CrossDrive by Karl Storz GmbH & Co. KG — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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USS — Synthes · Class I
Whistler Modular Pedicle Screw System — EVOLUTION SPINE, LLC · Class I
CosmoLock Pedicle Screw System — Kalitec Direct LLC · Class I

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: Karl Storz GmbH & Co. KG

Sources (1)

FDA UDI 0ae88a45-ed37-44d7-a9db-ff85ab669c7f 33 fields · synced Jun 6, 2026