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Pharmatech SRL

Italyfrom SRN

Devices
2

What Pharmatech SRL makes

Pharmatech Srl manufactures the REGEN2 and REGEN1 devices, which appear to be medical products designed for regenerative or tissue-engineering applications, likely intended for soft tissue or wound healing. These devices are formulated to support cellular regeneration or integration with biological tissues, potentially used in surgical or dermatological procedures.

The company’s portfolio is classified under EU Device Class IIa, indicating moderate risk and requiring compliance with EU MDR regulations. These devices are registered in the EU’s eudamed database, a centralised system for medical device information, and the manufacturer is based in Italy.

AI-generated from registry data, 20 Sep 2026. Not verified by deviCERTS or the manufacturer.

Catalogue2

Newest first, rows 1-2 of 2

  • REGEN2

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa
  • REGEN1

    Active Regimes: CE MDR Registry: EUDAMED Class:IIa

Frequently asked questions

How many devices does PHARMATECH SRL have in the registry?

The registry currently lists 2 devices for PHARMATECH SRL. Devices recorded under merged duplicate company entries are counted once.

Which registries list PHARMATECH SRL's devices?

Among its 2 most recently registered devices, PHARMATECH SRL has devices listed in EUDAMED (2 devices).

What risk classes do PHARMATECH SRL's devices fall under?

Among its 2 most recently registered devices, the classes recorded for PHARMATECH SRL's devices are Class IIa. Each device page shows its own class and authorisation.

What are the newest devices from PHARMATECH SRL in the registry?

The most recently registered devices listed for PHARMATECH SRL include REGEN2 and REGEN1.

Generated automatically from registry data and not verified by a human reviewer.