Microbiol S.r.l.
Italy IT-MF-000052547 Last updated 17 Sep 2026
- Devices
- 89
- Registries
- EUDAMED
- FDA recalls
- 0
Catalogue
Columbia Agar CNA + Crystal Violet Ref 14.0153V
Brodo per la conservazione dei ceppi Ref 18.0343-1
Ureasi Rapid Test Ref K.301-120
ISO Sensitest Agar Ref 14.0027V
Triptosio Agar Ref 14.0070V
Campy Plus Selective Broth Ref 18.0016-1
Thioglycollate Medium USP Ref 18.0085
Trichomonas Broth Mod. Ref 18.0084
HP Selective Agar Ref 14.0109V
Streptococco Latex Kit Gruppo A Ref O.10.70
Schadler Agar + CNA Ref 14.0062V
Carbaenterocromo Agar Ref 14.0684V
Todd Hewitt Broth Ref 18.0090
Coagulase Test Ref M.10.33
Rappaport Vassiliadis Soya Broth RV Ref 18.0083
Mac Conkey Agar with Crystal Violet Ref 14.0030V
C.L.E.D. Agar Ref 14.0016V
Salmonella Detection Agar Ref 14.0171V
Mueller Hinton AGar +4% NaCl +Oxacillina Ref 14.0046V
Mycoplasma Agar A7 Ref 60.123V
Mueller Hinton Agar +5% sangue cavallo +bNADdntone + Ref 14.0665V
Ureasi Rapid Test Ref K.301
Todd Hewitt CNA Broth Ref 18.0138
Sabouraud Dextrose Broth + CAF Ref 18.0051
Tryptone Soy Agar +5% sangue montone Ref 14.0074V
Tryptone Soy Agar Ref 14.0069V
Campy Plus Selective Broth Ref 18.0016
Candida Chromogenic Agar Ref 14.0178V
Malassezia (Dixon's) Selective Agar Ref 14.0193V
Clostridium Difficile Agar Ref 14.0015V
Sabouraud Dextrose Agar +CAF Ref 14.0051V
Sabouraud Dextrose Agar + CAF + GENT Ref 14.0054V
Streptococco Latex Kit Ref O.10.60
Sabouraud Dextrose Agar Broth USPe Ref 18.0050
Coagulase Test Ref M.10.32
Schaedler Agar +Sangue+neomicina+vancomicina Ref 14.0191V
Bile Esculina Agar Ref 14.0012V
Corynebacterium Selective Agar Ref 14.0358V
Salmonella Chromogenic Agar Ref 14.0158V
HP Transport Broth Ref K.315
Showing 51-90 of 89
About
30 years experience in the production and sale of diagnostics for use microbiologico
What Microbiol S.r.l. makes
Microbiol S.r.l. produces microbiological culture media and selective agars for identifying and isolating specific bacteria, including Weil Felix, Burkholderia cepacia, Gardnerella vaginalis, and Pseudomonas aeruginosa. Their portfolio also includes specialized media like thioglycollate broth with added vitamins, chocolate agar with bacitracin, and agar formulations for detecting antibiotic-resistant strains such as MRSA and VRE. Additional products include Gram staining kits and blood-enriched agar plates for general bacterial culture.
All listed microbiological media and diagnostic products fall under EU Class A medical devices and are registered in the EUDAMED database. The company is based in Italy and adheres to regulatory requirements for in vitro diagnostic (IVD) and microbiological culture media under EU regulations.
Frequently asked questions
What types of medical devices does Microbiol S.r.l. manufacture?
Microbiol S.r.l. specializes in microbiological culture media and selective agars designed for identifying and isolating specific bacteria. Their products include media like Weil Felix, Burkholderia cepacia selective agar, and Gardnerella vaginalis agar, as well as specialized formulations such as thioglycollate broth with added vitamins and antibiotics, chocolate agar with bacitracin, and agars for detecting antibiotic-resistant strains like MRSA and VRE. These devices are primarily used in clinical microbiology labs for diagnostic purposes.
Where is Microbiol S.r.l. based, and how does this affect its regulatory compliance?
Microbiol S.r.l. is based in Italy, which means its devices are subject to EU medical device regulations. Since all its microbiological media and diagnostic products fall under EU Class A medical devices, they must comply with EU regulatory requirements for in vitro diagnostics (IVDs) and microbiological culture media. This includes registration in the EUDAMED database, ensuring traceability and adherence to EU standards for safety and performance.
Which regulatory registries list Microbiol S.r.l.’s devices, and why is this important?
Microbiol S.r.l.’s devices are listed in the EUDAMED database, which is the European Union’s central registry for medical devices. This registry ensures transparency and traceability of devices placed on the EU market, allowing healthcare professionals, regulators, and authorities to verify the legitimacy and compliance status of the listed products. Being listed here confirms that the devices meet EU regulatory requirements, though individual device authorization is determined separately.
How are Microbiol S.r.l.’s devices classified under EU regulations, and what does this mean?
All of Microbiol S.r.l.’s microbiological culture media and diagnostic products are classified as EU Class A medical devices. This classification applies to low-risk devices, such as microbiological media used for identifying bacteria in controlled laboratory settings. Class A devices typically undergo less stringent regulatory scrutiny compared to higher-risk classes, but they still must comply with essential safety and performance requirements to ensure their intended use is met without posing undue risks to patients or users.
Information
- Country
- Italy
- Address
- snc, Zona Ind.le Macchiareddu VII Strada Ovest , UTA , Italy
- Website
- www.microbiol.it
- [email protected]
- Phone
- +39 070 247162
- PRRC contact
- Andrea Murgia
- EUDAMED SRN
- IT-MF-000052547