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Vytil

by Jiangsu Power-endo Medical Technology Co., Ltd 33 variants

Ref VTL/BUMPER-PE-S-20Model ENDO-BM, VTL/BUMPER

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, self-declared

Class I: no certifier involved

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 Number697559785PE10U5 Basic UDI-DI 06975597853213UDI-DIDate25 Apr 2025RegisteredStatusActive

Certificates

0 certificates · EUDAMED

No certifier certificate is listed. Devices of this class are self-declared by the manufacturer.

Coverage

1 jurisdiction

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  • Withdrawn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

European Union — CE/MDR Active

Specification

EUDAMED

Device Name
Disposable Scope Bumper
Model / Reference
ENDO-BM, VTL/BUMPER, VTL/BUMPER-PE-S-20
Primary DI / UDI-DI
06975597853213
Basic UDI-DI
697559785PE10U5
EMDN Code
T030101 Cover caps, instruments and equipment
Device Class
Class I
EU market of registration
France

Manufacturer details

EUDAMED SRN
CN-MF-000030213
Authorised representative
RIOMAVIX SOCIEDAD LIMITADA ES-AR-000001202

Other devices from Jiangsu Power-endo Medical Technology Co., Ltd

See all devices from Jiangsu Power-endo Medical Technology Co., Ltd →

Properties

Other properties (13)

  • Sterile: 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