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BenQ

by BenQ Medical Technology Corp. 33 variants

Ref 31SB-7R0B4-000Model Dr. Max 7000S

Active European Union

CE MDR

Valid until

Not listed

EUDAMED holds no validity date

FDA recalls

Not applicable

No FDA record for this device

Documents

None linked in EUDAMED

A group certificate may exist

Trust

Unverified

Registry data, not yet checked by deviCERTS. Source EUDAMED, synced 24 Oct 2026. What this means

Regulatory status

as of registry sync 24 Oct 2026

RegionAuthorizationNumberDateStatus
European UnionCE/MDR Number471987988DrMax700093 Basic UDI-DI 04719879882292UDI-DIDate25 Sep 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.

Coverage

1 jurisdiction

SwedenFinlandLatviaEstoniaDenmarkLithuaniaIrelandNetherlandsGermanyPolandFranceBelgiumLuxembourgCzech RepublicSlovakiaAustriaHungaryRomaniaSloveniaBulgariaPortugalSpainItalyCroatiaGreeceMaltaCyprus
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
"BenQ" Operating Tables and Accessories(Non-Sterile)
Model / Reference
Dr. Max 7000S, 31SB-7R0B4-000
Primary DI / UDI-DI
04719879882292
Basic UDI-DI
471987988DrMax700093
EMDN Code
Z12011202 Operating tables
Device Class
Class I
EU market of registration
Bulgaria

Manufacturer details

EUDAMED SRN
TW-MF-000012212
Authorised representative
MedNet EC-REP GmbH DE-AR-000000002

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Properties

  • Reusable

Other properties (12)

  • Sterile: No
  • Implantable: 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