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Robooter Q40

by Jiangsu Bangbang Intelligent Technology Co., Ltd.

Ref BBR-Q40-05Model BBR-Q40

Active European Union. Also listed in GUDID (US).

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

None found

in data synced 25 Oct 2026

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, GUDID, synced 25 Oct 2026. What this means

Regulatory status

as of registry sync 25 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing GUDID Number06978246580270 UDI-DI Date10 Sep 2026ListedStatusListed GUDID: in commercial distribution
European UnionCE/MDR EUDAMED Number697824658MS6W Basic UDI-DI Date8 Apr 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

EUDAMED lists no certificate for this device's Basic UDI-DI.

A certificate issued for a device group may exist without being linked here.

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 25 Oct 2026.

Coverage

2 jurisdictions

United States of AmericaSwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered
  • European Union CE/MDR Active
  • United States GUDID listing Listed

Specification

EUDAMED · GUDID

Trade Name
Robooter Q40 EUDAMED
Mobility Scooter (Robooter Q40) GUDID
Generic Name
Assistive scooter, electric-motor-driven
Device Name
Go Go Compact、Mobility Scooter (Robooter Q40)
Model / Reference
BBR-Q40, BBR-Q40-05
Primary DI / UDI-DI
06978246580270, 06978246580232, 06978246580454, 06978246580416, 06978246580393
Basic UDI-DI
697824658MS6W
Direct Marketing DI
06978246580270
06978246580232
06978246580454
06978246580416
06978246580393
510(k) Number
FDA Product Code
INI
EMDN Code
Y122124 Electric scooters
GMDN Term
Assistive scooter, electric-motor-driven
Device Class
Class I EUDAMED
Class II GUDID
Regulation Number
890.3800
EU market of registration
Northern Ireland
France
GUDID distribution status
In Commercial Distribution

Truth per registry

2 sources · 1 field differs

FieldEUDAMEDGUDID
Device ClassEUDAMED
Class I
GUDID
Class II

Manufacturer details

EUDAMED SRN
CN-MF-000046169
Authorised representative
SUNGO Europe B.V. NL-AR-000000247

Other devices from Jiangsu Bangbang Intelligent Technology Co., Ltd.

See all devices from Jiangsu Bangbang Intelligent Technology Co., Ltd. →

Properties

  • Lot / Batch Number
  • Serial Number
  • Expiration Date
  • Manufacturing Date

Other properties (20)

  • Sterile: No
  • Single Use: No
  • Implantable: No
  • Reusable: No
  • Contains Latex: No
  • Reprocessed: No
  • CMR Substance: No
  • Human-derived: No
  • Human Tissues: No
  • Animal Tissues: No
  • Endocrine Disruptor: No
  • Administering Medicine: No
  • Measuring Function: No
  • Incorporates Medicinal Product: No
  • Prescription Use: No
  • Over-the-Counter: No
  • Convenience Kit: No
  • Combination Product: No
  • HCT/P: No
  • Premarket Exempt: No