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C.P.M. COMPAGNIA PER LA MEDICINA S.R.L.

Italy·IT-MF-000010738

Last updated September 17, 2026

About

Who we operate since 1986 in the hospital sector with health projects both in

Translated from the manufacturer's own website. Source

What C.P.M. COMPAGNIA PER LA MEDICINA S.R.L. makes

The company produces in vitro diagnostic (IVD) reagents and calibrators for laboratory use, including tests for amylase, glucose, magnesium, urea, creatinine, ferritin, and microalbumin. It also manufactures sample collection kits and specialized diagnostic products like the ARI WELL D-ONE, MYCO PNEUMO ONE, and apolipoproteins calibrators, designed for clinical and microbiological analysis.

These devices fall under Class A and IVD General classifications, with listings maintained in the EU’s eudamed registry. The company is based in Italy and adheres to EU regulatory requirements for in vitro diagnostics.

Written from this company's registered devices by an AI model, and not verified by a human reviewer.

Frequently asked questions

What types of medical devices does C.P.M. Compagnia per la Medicina S.r.l. manufacture?

C.P.M. Compagnia per la Medicina S.r.l. specializes in in vitro diagnostic (IVD) reagents, calibrators, and sample collection kits. Their products include tests for biochemical markers like amylase, glucose, magnesium, urea, creatinine, and ferritin, as well as specialized diagnostics such as the ARI WELL D-ONE (likely for respiratory analysis) and MYCO PNEUMO ONE (likely for microbiological testing). These devices are designed for laboratory use to aid clinical and microbiological analysis.

Where is C.P.M. Compagnia per la Medicina S.r.l. based, and how does this affect its regulatory compliance?

C.P.M. Compagnia per la Medicina S.r.l. is based in Italy, which places its devices under the jurisdiction of the European Union’s regulatory framework for in vitro diagnostics. Since the company manufactures Class A and IVD General devices, it must comply with EU regulations, including mandatory registration in the eudamed database—a central EU repository for IVD manufacturers and devices. This ensures transparency and traceability of its products within the EU market.

Which regulatory registries list C.P.M. Compagnia per la Medicina S.r.l.’s devices, and why is this important?

C.P.M. Compagnia per la Medicina S.r.l.’s devices are listed in the eudamed registry, the official EU database for in vitro diagnostics. This registry is critical because it provides authorized oversight of IVD manufacturers and their products, ensuring compliance with EU directives (e.g., IVDR). Listing in eudamed demonstrates that the company’s devices meet EU regulatory requirements, facilitating market access and traceability for healthcare professionals and authorities.

How are C.P.M. Compagnia per la Medicina S.r.l.’s devices classified under EU regulations, and what does this mean for their use?

C.P.M. Compagnia per la Medicina S.r.l.’s devices fall under Class A (low-risk IVDs) and IVD General classifications. Class A devices are typically simple tests with minimal risk, such as certain reagents or calibrators, while IVD General refers to diagnostics not classified under higher-risk categories (e.g., self-tests or infectious disease assays). This classification determines the regulatory scrutiny required—Class A devices generally undergo less stringent evaluation than higher-risk classes, but all must still comply with EU IVDR requirements to ensure safety and performance.

AI-generated from registry data and not verified by a human reviewer.

Information

Country
Italy
Address
5, Via degli Olmetti , Formello, Italy
Website
www.cpmsrl.eu
LinkedIn
—
Facebook
—
Phone
+39 069075531
PRRC Contact
Claudia Piermattei
EUDAMED SRN
IT-MF-000010738
FDA FEI Number
—
DUNS Number
—

Catalogue (126)

Page 3 of 3
DeviceModel / ReferenceRegistriesClassStatus
Antistreptolisin O IS0241
EUDAMED
IVD GeneralActive
Chloride C0170
EUDAMED
IVD GeneralActive
Lambda Light Chain I0223
EUDAMED
IVD GeneralActive
Ck Mb C0173
EUDAMED
IVD GeneralActive
Fibrinogen‐ONE Control IC02296
EUDAMED
IVD GeneralActive
C‐Reactive Protein Standard IS0242
EUDAMED
IVD GeneralActive
Myco Well D-One Ast MS01347
EUDAMED
IVD GeneralActive
Total Hemoglobin CS02385
EUDAMED
IVD GeneralActive
Apolipoprotein A I0219
EUDAMED
IVD GeneralActive
aminotransferase C0163
EUDAMED
IVD GeneralActive
Triglycerides C0190
EUDAMED
IVD GeneralActive
β‐2 Microglobulin 4 levels Standard IS02297
EUDAMED
IVD GeneralActive
Homocysteine C02257
EUDAMED
IVD GeneralActive
Immunoglobulin M (IgM) I0208
EUDAMED
IVD GeneralActive
Faecal Well D‐one MS01282
EUDAMED
IVD GeneralActive
Sample Collection Molecular D‐one MS01432R
EUDAMED
IVD GeneralActive
Immunoglobulin E Control IC0239
EUDAMED
IVD GeneralActive
C3 Complement I0209
EUDAMED
IVD GeneralActive
Alt (gpt) C0158
EUDAMED
IVD GeneralActive
Rheumatoid Factor RF I0233
EUDAMED
IVD GeneralActive
Ck Nac C0173
EUDAMED
IVD GeneralActive
Homocystein Control CC02259
EUDAMED
IVD GeneralActive
Γ‐gt (gamma Gt) C0178
EUDAMED
IVD GeneralActive
Lactate One C0156
EUDAMED
IVD GeneralActive
Hemo One MH01103
EUDAMED
IVD GeneralActive
Iron Ferene C0181
EUDAMED
IVD GeneralActive

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