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Our data is continuously updated and sourced from EUDAMED, the European database for medical devices and in vitro diagnostics.

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VBM Medizintechnik GmbH

Certificate G10 016389 0029

Rev. Rev. 01IssuedExpiring soon
Valid until
Aug 23, 2026

Overview

Certificate number
G10 016389 0029
Certificate type
Quality management system
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
0123G10 016389 0029Rev. 01

Validity

Issued
Aug 3, 2023
Valid from
Aug 3, 2023
Valid until
Aug 23, 2026

Notified body

Notified body
TÜV SÜD Product Service GmbH
Notified body SRN
0123
Notified body country
Germany

Covered devices

No specific devices are listed for this certificate.

Characteristics

Sterile
Yes
Human tissues
No
Animal tissues
No
In vitro diagnostics
No
Initial registration
Yes
New device
No
Discard allowed
No
SSCP enabled
Yes
Mechanism of scrutiny
No
Intended medical purpose
No
SPP applicable
No
Conditions applicable
No
MOS outside EUDAMED
—
QMS/MOS type
Others

History

No status changes or preceding certificates are recorded.

Scope coverage

Class IIa10

10 scopes

  • R010202 - LARYNGEAL TUBES
    Class IIa
  • R010380 - ENDOTRACHEAL TUBES - ACCESSORIES
    Class IIa
  • R010699 - PERCUTANEOUS TRACHEOSTOMY KITS - OTHER
    Class IIa
  • R020101 - STANDARD BREATHING CIRCUITS
    Class IIa
  • R020201 - FIXED CATHETER MOUNTS
    Class IIa
  • R020202 - MOBILE CATHETER MOUNTS
    Class IIa
  • R0203 - ANAESTHESIA AND RESUSCITATION CONNECTORS
    Class IIa
  • R030101 - VENTILATION MASKS
    Class IIa
  • R030202 - MANUALLY OPERATED VENTILATION BALLOONS
    Class IIa
  • Z12139006 - PNEUMATIC TOURNIQUETS
    Class IIa

Documents

LanguagesEN

Manufacturer

Manufacturer
VBM Medizintechnik GmbH
Manufacturer SRN
DE-MF-000005907
Manufacturer country
Germany