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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

Interrad Medical, Inc.

Certificate 28620239803

Issued
Valid until
Dec 18, 2029

Certificate 28620239803 is a valid Technical documentation issued to Interrad Medical, Inc. and registered in EUDAMED. Valid until December 18, 2029. View the full certificate record on MD Atlas.

Overview

Certificate number
28620239803
Certificate type
Technical documentation
Certificate status
Issued
Applicable legislation
MDR [Regulation (EU) 2017/745 on medical devices]
Version
1
Certificate ID
286228620239803

Validity

Issued
Mar 6, 2026
Valid from
Mar 6, 2026
Valid until
Dec 18, 2029

Notified body

Notified body
Intertek Medical Notified Body AB
Notified body SRN
2862
Notified body country
Sweden

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
Yes
MOS outside EUDAMED
—
QMS/MOS type
Others

History

No status changes or preceding certificates are recorded.

Scope coverage

Unspecified1

1 scope

  • SecurAcath
    08653820002400XXXG5

Documents

LanguagesEN

Manufacturer

Manufacturer
Interrad Medical, Inc.
Manufacturer SRN
US-MF-000009878
Manufacturer country
United States

Covered devices

  • SecurAcathClass IIb
    08653820002400XXXG5

Linked SSCPs

  • SSCP 1438-005