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Drivemedical

FDA UDI

Class I (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name
DRIVEMEDICAL FDA UDI
Generic Name
Portable ramp FDA UDI
Device Name
Transport/WheelchairAccessories Product Description: Oxygen Tank Holder/IV Pole1/cs FDA UDI
Model / Reference
STDS804 FDA UDI
Description
Transport/WheelchairAccessories Product Description: Oxygen Tank Holder/IV Pole1/cs FDA UDI

Identifiers

Primary DI / UDI-DI
00822383106946 FDA UDI
FDA Product Code
KNO FDA UDI
GMDN Term
Portable ramp FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3910 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

No

FDA UDI

Serial Number

Yes

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 e3f50824-5320-4c8f-a31a-b56f2c9a5003 34 fields · synced Jun 8, 2026