Medical Products Research
Italy IT-MF-000025583 Last updated 21 Oct 2026
- Devices
- 80
- Registries
- EUDAMEDFDA
- FDA recalls
- 0
Catalogue
Lifeflow Efa® Ref MPR904
Tpep®avant Ref MPR205
Ie Plus Ref MPR404
Flowtherm 60 Efa® Ref MPR902
Kfa/F Ref KFA/F
MPR700 - Tpep® Advanced I/E Ref MPR700
Kalos Ref MPR402
Tpep® One Ref MPR710
Kvak Ref KVAK
Dysph-Aide Ref MPR802
Uniko-Tpep® E Ref MPR200
Unikit Ref UNIKIT
Khfl/A Ref KHFL/A
MPR713 Ref MPR713
Free Aspire Advanced Ref MPR600
Kvak/S Ref KVAK/S
H-Flow Ref MPR918
Kfah/Fa Ref KFAH/FA
MPR201 Ref MPR201
Suction Free Compressor Ref MPR231
Free Flow Ref MPR900
Free Aspire Ref MPR100/M
Khfl/Cm Ref KHFL/CM
Khfl/Cm Ref KHFL/CM
MPR282 Ref MPR282
MPR712 Ref MPR712
Tpep® 4 Ref MPR708
Kvak/V Ref KVAK/V
MPR714 Ref MPR714
Khfl/Ca Ref KHFL/CA
MPR202 Ref MPR202
MPR345UK Ref MPR345UK
Lifeflow Ref MPR908
Flow Kleaner Ref MPR807
Kfaa Ref KFAA
Kvak/Fa Ref KVAK/FA
Tpep®advanced I/E Ref MPR280
MPR208 Ref MPR208
Kvak/Sv Ref KVAK/SV
Kinex Ref MPR410
MPR715 Ref MPR715
Khfl/Hfa Ref KHFL/HFA
Kfah Ref KFAH
Futura Ref MPR10-03BAS-00
Libera Pro + MPR10-00KIT-01 Ref MPR10-01PRO-01
Micol Pro Ref MPR10-02PRO-00
Micol Ref MPR10-02BAS-00
Inext Com Ref MPR10-04COM-00
Libera + MPR10-00KIT-01 Ref MPR10-01BAS-01
Micol Sat Ref MPR10-02SAT-00
Showing 1-50 of 80
EUDAMED certificates
ICIM S.P.A. 0425 2 certificates
- 0425-MDR-030143-00 Issued
Quality management system EU MDR
- Issued
- 5 Aug 2025
- Expires
- 4 Aug 2030
- 0425-MDR-030128-00 Issued
Quality management system EU MDR
- Issued
- 14 Mar 2025
- Expires
- 13 Mar 2030
Related companies
Notified bodies
- ICIM S.P.A. 0425
FDA establishments
- Medical Products & Research, Inc. US
About
Medical Products Research Srl+39 0331 597992Via Novara, 68, 20025 Legnano MIP.IVA [email protected]
What Medical Products Research makes
Medical Products Research manufactures a range of Class IIa medical devices primarily focused on patient monitoring and diagnostic imaging solutions. Their portfolio includes devices such as the MICOL series (MICOL PRO, MICOL SAT), which appear to be ultrasound-based diagnostic tools, as well as the INEXT series (INEXT PRO, INEXT COM) likely used for imaging or procedural guidance. Additional products like the LIBERA series (LIBERA PRO, LIBERA SAT) and FRIDA COM suggest specialized imaging or diagnostic equipment, while the ATENA70 series (ATENA70 SAT, ATENA70 COM) may cater to specific medical imaging applications.
All listed devices fall under EU Class IIa classification and are registered in the EUDAMED database, adhering to European medical device regulations. The company is based in Italy, where its products are subject to compliance with EU Medical Device Regulation (MDR) requirements.
Frequently asked questions
What types of medical devices does Medical Products Research manufacture?
Medical Products Research specializes in Class IIa medical devices, primarily focused on patient monitoring and diagnostic imaging. Their product range includes ultrasound-based tools like the MICOL series (e.g., MICOL PRO, MICOL SAT) and imaging/guidance devices such as the INEXT series (e.g., INEXT PRO, INEXT COM). Other products, like the LIBERA and ATENA70 series, appear tailored for specialized diagnostic or imaging applications, ensuring compliance with EU medical device regulations.
Where is Medical Products Research based, and how does this affect its devices?
Medical Products Research is based in Italy, which means its devices are subject to European Union Medical Device Regulation (MDR) requirements. Being based in the EU ensures alignment with EUDAMED registration and compliance standards, as all listed devices are recorded in the EUDAMED database under Class IIa classification.
Which regulatory registries list Medical Products Research’s devices?
Medical Products Research’s devices are listed in the EUDAMED database, which is the official European Union registry for medical devices. This registry tracks compliance and authorisation details for devices under EU regulations, including those classified as Class IIa.
How are Medical Products Research’s devices classified under EU regulations?
All devices manufactured by Medical Products Research fall under the EU Class IIa classification. This classification is determined based on risk assessment criteria outlined in EU Medical Device Regulation (MDR), indicating a moderate risk level that requires compliance with specific safety and performance standards before market placement.
Information
- Country
- Italy
- Address
- 7, Piazza San Magno, Legnano, Italy
- Website
- www.mpr-italy.it/
- facebook.com/mpritaly
- [email protected]
- Phone
- +39 0331 1404562
- EUDAMED SRN
- IT-MF-000025583