Clutch Drill

FDA UDI

Class I (US FDA UDI)

by Sweden & Martina Inc

Identity

Trade Name: CLUTCH DRILL FDA UDI
Generic Name: Screw extractor, reusable FDA UDI
Device Name: CLUTCH DRILL FOR REMOVAL SCREW KIT FDA UDI
Model / Reference: FA-EXTRACTOR FDA UDI
Description: CLUTCH DRILL FOR REMOVAL SCREW KIT FDA UDI

Identifiers

Catalog Number: FA-EXTRACTOR FDA UDI
Primary DI / UDI-DI: D7700614863 FDA UDI
FDA Product Code: NDP FDA UDI
GMDN Term: Screw extractor, reusable FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 872.3980 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

Yes

FDA UDI

Expiration Date

FDA UDI

Manufacturing Date

FDA UDI

Sterilization Method

Moist Heat or Steam Sterilization FDA UDI

Category: Screw extractor, reusable

Clutch Drill by Sweden & Martina Inc — 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: Sweden & Martina Inc

Sources (1)

FDA UDI 25823df9-59d1-46ca-a320-e9dc0fd629ae 35 fields · synced May 30, 2026