Interrad Medical, Inc.
Active in EUDAMEDUnited Statesfrom SRN EUDAMED SRN US-MF-000009878
- Devices
- 13
- Registrations
- EUDAMED
At a glance
EU certificates
1 of 1 in force.
Market reach
- European Union
- EUDAMED actor, 1 certificate
- Authorised rep.
- MDSS GmbHDE
Catalogue
SecurAcath Ref 400170
SecurAcath 12F Ref 12F
SecurAcath 8F Ref 8F
Securacath Universal Ref K092306
Securacath Catheter, Model SPK01 Ref K082047
Modification To Securacath, Model: SPK01 Ref K083081
SecurAcath Ref 400180
SecurAcath Ref 400120
SecurAcath Ref 400150
SecurAcath Ref 400130
SecurAcath Ref 400140
SecurAcath Ref 400110
Company details
- EUDAMED SRN
- US-MF-000009878
- DUNS number
- 555472310
- EU VAT number
- 32-0021678
- EUDAMED status
- Active
- EUDAMED registered name
- Interrad Medical, Inc.
- EUDAMED abbreviated name
- Interrad
- Registered address
- 181, Cheshire Lane, 55441, Plymouth, United States
- Website
- www.securAcath.com
- linkedin.com/company/1637121
- facebook.com/securacath
- [email protected]
- Phone
- +1 763 225 6699
- PRRC contact
- Denise Lenz
EUDAMED certificates
1 certificate1 valid, 0 expiredMDR 1next expiry 18 Dec 2029
Intertek Medical Notified Body AB 2862 1 certificate
- 28620239803 Issued
Technical documentation EU MDR
- Issued
- 6 Mar 2026
- Expires
- 18 Dec 2029
From the company website
SecurAcath® delivers dramatic reduction in catheter dislodgement 6 comparative studies 5 countries 12,815 patients Neonates to geriatrics Over 1.5 million catheter days Data pooled from Hawes 2023, McParlan 2020, Dolcino 2017, Kleidon 2024, Goossens 2018, and Pittiruti 2022 SecurAcath® provides a significant reduction in risk of CLABSI UAMS
Frequently asked questions
How many devices does Interrad Medical, Inc. have in the registry?
The registry currently lists 13 devices for Interrad Medical, Inc.. Devices recorded under merged duplicate company entries are counted once.
Which registries list Interrad Medical, Inc.'s devices?
Among its 13 most recently registered devices, Interrad Medical, Inc. has devices listed in EUDAMED (9 devices), FDA 510(k) (4 devices) and FDA GUDID (8 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do Interrad Medical, Inc.'s devices fall under?
Among its 13 most recently registered devices, the classes recorded for Interrad Medical, Inc.'s devices are Class I, Class IIb and Class II. Each device page shows its own class and authorisation.
What EUDAMED certificates are recorded for Interrad Medical, Inc.?
EUDAMED lists 1 certificate for Interrad Medical, Inc. (technical documentation) under MDR. 1 is recorded with the status issued. The most recent was issued on 2026-03-06.
What are the newest devices from Interrad Medical, Inc. in the registry?
The most recently registered devices listed for Interrad Medical, Inc. include SecurAcath, SecurAcath 12F, SecurAcath 8F and SECURACATH UNIVERSAL.