Drive

FDA UDI

Class I (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name: Drive FDA UDI
Generic Name: Assistive manual gripping tongs FDA UDI
Device Name: Personal CareAids to Daily Living Product Description: Infrared Heat Wand, Rtl. 1/bx FDA UDI
Model / Reference: 10-65200 FDA UDI
Description: Personal CareAids to Daily Living Product Description: Infrared Heat Wand, Rtl. 1/bx FDA UDI

Identifiers

Primary DI / UDI-DI: 00822383210681 FDA UDI
FDA Product Code: ISA FDA UDI
GMDN Term: Assistive manual gripping tongs FDA UDI

Classification

Device Class: Class I FDA UDI
Regulation Number: 890.5660 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

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

FDA UDI

Manufacturing Date

FDA UDI

Category: Assistive manual gripping tongs

Drive by Drive Devilbiss Healthcare — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

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DRIVEMEDICAL — Drive Devilbiss Healthcare · 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: Drive Devilbiss Healthcare

Sources (1)

FDA UDI 19545d77-7cc1-4b59-a1fa-bafcbf311c19 33 fields · synced Jun 8, 2026