Medical Screwdriver (SD 2)

FDA UDI

Class I (US FDA UDI)

by Med-El Elektromedizinische Geräte Gesellschaft m.b.H.

Identity

Trade Name: Medical Screwdriver (SD 2) FDA UDI
Generic Name: Surgical screwdriver, single-use FDA UDI
Device Name: Single-Use Surgical Tool FDA UDI
Model / Reference: 52790 FDA UDI
Description: Single-Use Surgical Tool FDA UDI

Identifiers

Primary DI / UDI-DI: 09008737527907 FDA UDI
FDA Product Code: LRC FDA UDI
GMDN Term: Surgical screwdriver, single-use FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 874.4420 FDA UDI
Commercial Distribution: In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

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

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Surgical screwdriver, single-use

Medical Screwdriver (SD 2) by Med-El Elektromedizinische Geräte Gesellschaft m.b.H. — 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: Med-El Elektromedizinische Geräte Gesellschaft m.b.H.

Sources (1)

FDA UDI 0f665908-3433-408f-bdc4-18c7f3d9bc7c 35 fields · synced Jun 1, 2026