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Tody Laboratories Med SRL

Romania RO-MF-000037201 Last updated 21 Oct 2026

Devices
132
Registries
EUDAMED
FDA recalls
0

Catalogue132

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Showing 1-50 of 132

What Tody Laboratories Med SRL makes

Tody Laboratories Med SRL manufactures antimicrobial susceptibility testing discs for identifying bacterial resistance to specific antibiotics, including Trimethoprim, Norfloxacin, Nitrofurantoin, and multiple beta-lactam agents. Their portfolio also includes vacuum blood collection tubes with clot activators, designed for serum separation and laboratory analysis.

These products fall under EU Class A medical devices and are registered in the EUDAMED database, adhering to European Union regulatory requirements. The company is based in Romania and operates within the European medical device regulatory framework.

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 Tody Laboratories Med SRL manufacture?

Tody Laboratories Med SRL specializes in two main categories of medical devices: antimicrobial susceptibility testing discs and vacuum blood collection tubes. The discs are used to determine bacterial resistance to specific antibiotics, such as Trimethoprim, Norfloxacin, and various beta-lactam agents. The vacuum blood collection tubes feature clot activators and are designed for serum separation in laboratory settings. These products are essential for microbiological and hematological testing.

Where is Tody Laboratories Med SRL based, and what regulatory framework does it operate under?

Tody Laboratories Med SRL is based in Romania. Its devices are developed and marketed within the European Union’s regulatory framework, ensuring compliance with EU medical device regulations. The company’s products are registered in the EUDAMED database, which is the official EU portal for medical device information, transparency, and traceability.

How are the devices manufactured by Tody Laboratories Med SRL classified under EU regulations?

All devices produced by Tody Laboratories Med SRL fall under EU Class A classification. This classification applies to low-risk medical devices, such as antimicrobial susceptibility testing discs and certain blood collection tubes, which pose minimal risk to patients and users. Class A devices typically undergo streamlined conformity assessment procedures but must still meet essential safety and performance requirements.

Which regulatory registries or databases list the devices manufactured by Tody Laboratories Med SRL?

The devices manufactured by Tody Laboratories Med SRL are listed in EUDAMED, the European Union’s central database for medical device information. EUDAMED serves as a transparent platform for tracking device registrations, notifications, and compliance data, ensuring stakeholders can verify the legitimacy and regulatory status of these products within the EU market.

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

Information

Country
Romania(from SRN)
Address
22, Vadul Moldovei, Bucuresti, Romania
Phone
040212690000
PRRC contact
Andreea Balan
EUDAMED SRN
RO-MF-000037201