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Drive

FDA UDI

Class I (US FDA UDI)

by Drive Devilbiss Healthcare

Identity

Trade Name
DRIVE FDA UDI
Generic Name
Axillary crutch FDA UDI
Device Name
Canes & Crutches Offset Product Description Cane, Offset Gel Grip, Floral, 1/ea,6/cv FDA UDI
Model / Reference
RTL10372FL FDA UDI
Description
Canes & Crutches Offset Product Description Cane, Offset Gel Grip, Floral, 1/ea,6/cv FDA UDI

Identifiers

Primary DI / UDI-DI
00822383000794 FDA UDI
FDA Product Code
IPS FDA UDI
GMDN Term
Axillary crutch FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3075 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

Yes

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

Drive 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 aea37816-8671-4044-b37d-8c676ea8255d 34 fields · synced Jun 8, 2026