← Back to catalogue

Valmax

FDA UDI

Class I (US FDA UDI)

by Supply Line Medical

Identity

Trade Name
Valmax FDA UDI
Generic Name
Manual traction wheelchair FDA UDI
Model / Reference
DME.014 FDA UDI

Identifiers

Primary DI / UDI-DI
00860014621802 FDA UDI
FDA Product Code
IOR FDA UDI
GMDN Term
Manual traction wheelchair FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
890.3850 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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Manual traction wheelchair

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

Similar devices

Also classified as Manual traction wheelchair.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Supply Line Medical

Sources (1)

  • FDA UDI 0a8c17fe-8305-495e-9773-00cc6e58a0d7 32 fields · synced May 30, 2026