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Drivemedical

FDA UDI

Class I (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name
DRIVEMEDICAL FDA UDI
Generic Name
Assistive shoehorn/bootjack FDA UDI
Device Name
Personal CareAids to Daily Living Product Description: PaddedDressingStick w/ShoeHorn,1EA,3/CS FDA UDI
Model / Reference
RTL2032 FDA UDI
Description
Personal CareAids to Daily Living Product Description: PaddedDressingStick w/ShoeHorn,1EA,3/CS FDA UDI

Identifiers

Primary DI / UDI-DI
00779709020328 FDA UDI
FDA Product Code
ILD FDA UDI
GMDN Term
Assistive shoehorn/bootjack FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.5050 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Assistive shoehorn/bootjack

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

Similar devices

Also classified as Assistive shoehorn/bootjack.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 075a5b81-2f1e-48a8-b642-c6b3f0be03bd 33 fields · synced Jun 8, 2026