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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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MD Atlas
Documents

D.R.M. S.R.L.

Certificate 55998

Rev. 0Issued

Valid until: Jan 24, 2028

Overview

Certificate number: 55998
Certificate type: Quality assurance
Certificate status: Issued
Applicable legislation: MDR [Regulation (EU) 2017/745 on medical devices]
Version: 1
Certificate ID: 0546559980

Validity

Issued: Jan 25, 2023
Valid from: Jan 25, 2023
Valid until: Jan 24, 2028

Manufacturer

Manufacturer: D.R.M. S.R.L.
Manufacturer SRN: IT-MF-000027115
Manufacturer country: Italy

Notified body

Notified body: CERTIQUALITY S.r.l.
Notified body SRN: 0546
Notified body country: Italy

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 I3

3 scopes

General non-active non-implantable devices used in health care and other non-active non-implantable devices.
Class I
Sterile general non-invasive dressing kits
Class I
Sterile peritoneal and extracorporeal dressing kits for use pre and post dialysis
Class I

Documents

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