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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: Anti-Fold/Theft Device for w/c,1/ea FDA UDI
Model / Reference
STDS806 FDA UDI
Description
Transport/WheelchairAccessories Product Description: Anti-Fold/Theft Device for w/c,1/ea FDA UDI

Identifiers

Primary DI / UDI-DI
00822383106953 FDA UDI
FDA Product Code
IMR FDA UDI
KNN FDA UDI
GMDN Term
Portable ramp FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3920 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: Portable ramp

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

Similar devices

Also classified as Portable ramp.

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 09299bbe-3f64-4138-9e17-66a024217766 33 fields · synced Jun 8, 2026