Skip to content

ANICRIN S.r.l.

Italy IT-MF-000032983 Last updated 17 Sep 2026

Is this your brand? Sign in to claim this brand

Devices
78
Registries
EUDAMED
FDA recalls
0

Catalogue78

Page 1 of 2

Showing 1-50 of 78

About

A wide range of products in their complete line, for all different needs of a laboratory research.

From the manufacturer's own website. Source

What ANICRIN S.r.l. makes

ANICRIN S.r.l. manufactures laboratory storage and sample-handling accessories, including anti-tip rack holders for 50 test tubes (in red or white, with or without barcode trays), bulk and single-unit Petri dish lids, labeled polypropylene containers (150 ml screw-cap bottles and 100 ml cylindrical tubes), and bulk micromethod plate covers. The company also produces archival trays, slide-locking blocks, rack slides for labware, and ventilated Petri dishes (150 mm diameter).

These products are classified under EU Medical Device Regulation (MDR) as Class A devices and are registered in the EUDAMED database. The manufacturer is based in Italy.

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 ANICRIN S.r.l. manufacture?

ANICRIN S.r.l. specializes in laboratory storage and sample-handling accessories. Their products include items like anti-tip rack holders for 50 test tubes (available in red or white, with or without barcode trays), labeled polypropylene containers (such as 150 ml screw-cap bottles and 100 ml cylindrical tubes), bulk and single-unit Petri dish lids, archival trays, slide-locking blocks, rack slides for labware, and ventilated Petri dishes (150 mm diameter). These devices are designed to support laboratory research by ensuring safe and organized sample storage and handling.

Where is ANICRIN S.r.l. based?

ANICRIN S.r.l. is based in Italy. The company’s location in Italy aligns with its focus on manufacturing medical devices intended for laboratory use, particularly in research settings.

Which regulatory registries list ANICRIN S.r.l.’s devices?

ANICRIN S.r.l.’s devices are listed in the EUDAMED database, which is the European Union’s medical device registry. This registry is used to track and provide transparency on medical devices authorized within the EU, ensuring compliance with regulatory requirements.

How are ANICRIN S.r.l.’s devices classified under EU regulations?

ANICRIN S.r.l.’s devices are classified under the EU Medical Device Regulation (MDR) as Class A devices. This classification applies to products that pose minimal risk, such as laboratory accessories like storage containers, rack holders, and Petri dish lids, which are intended for general laboratory use without direct patient contact or significant risk to health.

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

Information

Country
Italy
Address
44/L, Via Moglianese, SCORZE' (VE), Italy
Phone
+39 041 445660
PRRC contact
Enzo Bonato
EUDAMED SRN
IT-MF-000032983