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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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ANACONDA BIOMED, S.L.

Certificate 2266433TD01

Rev. Rev. 0Issued
Valid until
Jun 1, 2030

Certificate 2266433TD01 is a valid Technical documentation issued to ANACONDA BIOMED, S.L. and registered in EUDAMED. Valid until June 1, 2030. View the full certificate record on MD Atlas.

Overview

Certificate number
2266433TD01
Certificate type
Technical documentation
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
03442266433TD01Rev. 0

Validity

Issued
Jun 4, 2025
Valid from
Jun 4, 2025
Valid until
Jun 1, 2030

Notified body

Notified body
DEKRA Certification B.V.
Notified body SRN
0344
Notified body country
Netherlands

Characteristics

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

History

No status changes or preceding certificates are recorded.

Scope coverage

Unspecified1

1 scope

  • ANA5 Advanced Neurovascular Access
    8437019519ANAB6

Documents

LanguagesEN

Manufacturer

Manufacturer
ANACONDA BIOMED, S.L.
Manufacturer SRN
ES-MF-000009187
Manufacturer country
Spain

Covered devices

  • ANA5 Advanced Neurovascular AccessClass III
    8437019519ANAB6