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Valmax

FDA UDI

Class I (US FDA UDI)

by Supply Line Medical

Identity

Trade Name
Valmax FDA UDI
Generic Name
Wheelchair brake extension FDA UDI
Model / Reference
DME.076 FDA UDI

Identifiers

Primary DI / UDI-DI
00860013569822 FDA UDI
FDA Product Code
IMW FDA UDI
GMDN Term
Wheelchair brake extension 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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Wheelchair brake extension

Valmax by Supply Line Medical — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Wheelchair brake extension.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Supply Line Medical

Sources (1)

  • FDA UDI ff4ef8d0-0d3f-422e-bcad-e078248bec90 32 fields · synced Jun 8, 2026