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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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Joimax GmbH

Certificate G11 049319 0011

Rev. Rev. 00Issued
Valid until
Feb 4, 2029

Certificate G11 049319 0011 is a valid Quality management system issued to Joimax GmbH and registered in EUDAMED. Valid until February 4, 2029. View the full certificate record on MD Atlas.

Overview

Certificate number
G11 049319 0011
Certificate type
Quality management system
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
0123G11 049319 0011Rev. 00

Validity

Issued
Mar 22, 2024
Valid from
Mar 22, 2024
Valid until
Feb 4, 2029

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
No
Human tissues
No
Animal tissues
No
In vitro diagnostics
No
Initial registration
Yes
New device
No
Discard allowed
No
SSCP enabled
No
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 I2

2 scopes

  • L03 - GENERAL SURGERY INSTRUMENTS, REUSABLE
    Class I
  • L11 - NEUROSURGERY AND SPINAL SURGERY INSTRUMENTS, REUSABLE
    Class I

Documents

LanguagesEN

Manufacturer

Manufacturer
Joimax GmbH
Manufacturer SRN
DE-MF-000009201
Manufacturer country
Germany