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Drivemedical

FDA UDI

Class I (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name
DRIVEMEDICAL FDA UDI
Generic Name
Cast/bandage waterproof bathing cover, single-use FDA UDI
Device Name
Personal CareAids to Daily Living Product Description: Cast Protector,24.5" Leg, 1 PC/RTL,50/CV FDA UDI
Model / Reference
RTLPC23402 FDA UDI
Description
Personal CareAids to Daily Living Product Description: Cast Protector,24.5" Leg, 1 PC/RTL,50/CV FDA UDI

Identifiers

Primary DI / UDI-DI
00822383563176 FDA UDI
FDA Product Code
KIA FDA UDI
GMDN Term
Cast/bandage waterproof bathing cover, single-use FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.6185 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: Cast/bandage waterproof bathing cover, single-use

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

Similar devices

Also classified as Cast/bandage waterproof bathing cover, single-use.

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 b2b8c440-2c1f-4c58-a94a-dd5b8d94b0f0 33 fields · synced Jun 8, 2026