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Drivemedical

FDA UDI

Class I (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name
DRIVEMEDICAL FDA UDI
Generic Name
Gel-filled bed mattress FDA UDI
Device Name
Pressure PreventionLTC and Hospice Product Description: Spec.Furn.,Grav8 Mattress 80"w/RR,1/EA FDA UDI
Model / Reference
SPFREVADX80-RR FDA UDI
Description
Pressure PreventionLTC and Hospice Product Description: Spec.Furn.,Grav8 Mattress 80"w/RR,1/EA FDA UDI

Identifiers

Primary DI / UDI-DI
00822383548708 FDA UDI
FDA Product Code
IKY FDA UDI
GMDN Term
Gel-filled bed mattress FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
880.5150 FDA UDI
Commercial Distribution
Not 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

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

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 1472a63c-915f-4b2f-b8cf-e9ab14c6cff8 34 fields · synced Jun 8, 2026