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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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Laboratorio Aragó S.L.

Certificate 2025 DR 0061

Rev. 1Issued
Valid until
Jul 17, 2030

Overview

Certificate number
2025 DR 0061
Certificate type
Technical documentation
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
03182025 DR 00611

Validity

Issued
Sep 18, 2025
Valid from
Sep 18, 2025
Valid until
Jul 17, 2030

Manufacturer

Manufacturer
Laboratorio Aragó S.L.
Manufacturer SRN
ES-MF-000001958
Manufacturer country
Spain

Notified body

Notified body
CENTRO NACIONAL DE CERTIFICACION DE PRODUCTOS SANITARIOS
Notified body SRN
0318
Notified body country
Spain

Covered devices

  • Sutura de P.G.A. (ácido poliglicólico)Class III
    8427599DTTF0147C

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

  • Sutura de P.G.A. (ácido poliglicólico)
    8427599DTTF0147C

Documents

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