← Back to catalogue

Q6 Edge HD

EUDAMEDFDA UDI

Class I (EU MDR)

Ref Q6 Edge HD

by Pride Mobility Products Corporation

Identity

Trade Name
Q6 Edge HD EUDAMEDFDA UDI
Generic Name
Electric-motor-driven wheelchair, occupant-controlled FDA UDI
Device Name
Q6 Edge HD EUDAMED
A powered wheelchair is a battery-operated device with wheels that is intended for medical purposes to provide mobility to persons restricted to a sitting position. FDA UDI
Model / Reference
Q6 Edge HD EUDAMED
Q6 Edge HD/Q6 Edge HD with iLevel FDA UDI
Description
A powered wheelchair is a battery-operated device with wheels that is intended for medical purposes to provide mobility to persons restricted to a sitting position. FDA UDI

Identifiers

Catalog Number
N/A FDA UDI
Primary DI / UDI-DI
00606509200059 EUDAMEDFDA UDI
Basic UDI-DI
6065090060650920005*9G8 EUDAMED
Direct Marketing DI
00606509200059 EUDAMED
FDA Product Code
ITI FDA UDI
EMDN Code
Y122127 ELECTRIC WHEELCHAIRS EUDAMED
GMDN Term
Electric-motor-driven wheelchair, occupant-controlled FDA UDI

Classification

Device Class
Class I EUDAMED
Class II FDA UDI
Regulation Number
890.3860 FDA UDI
Market of Registration
Netherlands EUDAMED
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

EUDAMEDFDA UDI

Single Use

No

FDA UDI

Implantable

No

EUDAMEDFDA UDI

Reusable

No

EUDAMED

Contains Latex

No

EUDAMEDFDA UDI

Reprocessed

No

EUDAMED

CMR Substance

No

EUDAMED

Human-derived

No

EUDAMED

Human Tissues

No

EUDAMED

Animal Tissues

No

EUDAMED

Endocrine Disruptor

No

EUDAMED

Administering Medicine

No

EUDAMED

Measuring Function

No

EUDAMED

Incorporates Medicinal Product

No

EUDAMED

Prescription Use

Yes

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

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Q6 Edge HD by Pride Mobility Products Corporation — Class I — MDR, FDA UDI — listed in EUDAMED, FDA GUDID — regulatory data on deviCERTS

Authorization Coverage (2 countries)

Regulatory Authorizations

European Union Active

CE/MDR

United States Pending data

FDA UDI

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

Manufacturer

EUDAMED SRN
US-MF-000008467
Authorised Representative
Pride Mobility Products Europe BV NL-AR-000001684

Sources (2)

  • EUDAMED dd7e5a1a-2436-482b-b4e3-a3a392897bb6 61 fields · synced Jun 18, 2026
  • FDA UDI 2841c1ce-6a13-4f6b-bce9-e850976da623 34 fields · synced May 30, 2026