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Drivemedical

FDA UDI

Class I (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name
DRIVEMEDICAL FDA UDI
Generic Name
Lumbar cushion FDA UDI
Device Name
Personal CareAids to Daily Living Product Description: Inflatable Cushion,Rubber,Red,1EA,6/CS FDA UDI
Model / Reference
RTLPC23346 FDA UDI
Description
Personal CareAids to Daily Living Product Description: Inflatable Cushion,Rubber,Red,1EA,6/CS FDA UDI

Identifiers

Primary DI / UDI-DI
00822383283821 FDA UDI
FDA Product Code
KIC FDA UDI
GMDN Term
Lumbar cushion FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3175 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

Yes

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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Lumbar cushion

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

Similar devices

Also classified as Lumbar cushion.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Drive Devilbiss Healthcare

Sources (1)

  • FDA UDI 8d52bdcf-bfaf-407b-a2f4-ed5a5e9b764e 33 fields · synced Jun 8, 2026