← Back to catalogue

Solax

FDA UDI

Class II (US FDA UDI)

by Guangdong Prestige Technology Company Limited

Identity

Trade Name
Solax FDA UDI
Generic Name
Electric-motor-driven wheelchair, occupant-controlled FDA UDI
Device Name
Electric wheelchair FDA UDI
Model / Reference
S7018 FDA UDI
Description
Electric wheelchair FDA UDI

Identifiers

Primary DI / UDI-DI
06970990830519 FDA UDI
510(k) Number
K240270 FDA UDI
FDA Product Code
ITI FDA UDI
GMDN Term
Electric-motor-driven wheelchair, occupant-controlled FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
890.3860 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

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Unsafe FDA UDI

Category: Electric-motor-driven wheelchair, occupant-controlled

Solax by Guangdong Prestige Technology Company Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electric-motor-driven wheelchair, occupant-controlled.

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
Guangdong Prestige Technology Company Limited

Sources (1)

  • FDA UDI 3e055099-421a-4205-8f24-f72ad1eebd37 34 fields · synced May 29, 2026