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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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Meiji Pharma Spain, S.A.

Certificate 2024 CR 0026

Rev. 2Issued
Valid until
Jun 26, 2029

Overview

Certificate number
2024 CR 0026
Certificate type
Quality management system
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
03182024 CR 00262

Validity

Issued
Sep 11, 2024
Valid from
Sep 11, 2024
Valid until
Jun 26, 2029

Manufacturer

Manufacturer
Meiji Pharma Spain, S.A.
Manufacturer SRN
ES-MF-000001023
Manufacturer country
Spain

Notified body

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

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
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 III4

4 scopes

  • MDN 1102: Implantes óseos ortopédicos no activos / Non-active osteo-and orthopaedic implants
    Class III
  • Solución de hialuronato sódico 1% (10mg/ml) 2,5ml jeringa intraarticular / Sodium hyaluronate 1% (10 mg/ml) 2.5ml solution. Intra articular syringe
    Class III
  • Solución de hialuronato sódico 1% (10mg/ml) 4,9ml jeringa intraarticular / Sodium hyaluronate 1% (10 mg/ml) 4.9ml solution. Intra articular syringe
    Class III
  • Solución de hialuronato sódico 2% (20mg/ml) 4,9ml jeringa intraarticular / Sodium hyaluronate 2% (20 mg/ml) 4.9 ml solution. Intra articular syringe
    Class III

Documents

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