GOSSELIN is a family owned company which was created 45 years ago by Pierre Gosselin, PhD Pharmacist. ISO 9001 Certification version 2000 Construction of a dedicated site to Petri Plates manufacturing in a clean room.
Gosselin has always been turn towards research and innovation in order to satisfy all the user’s needs. In fact, the company has constantly created quality products according to the international standards in force. Gosselin brings its well known know-how through different scopes of application as food and pharmaceutical industry, medical analysis, environment, dairy and microbiology.
The Petri Plates range is large. Indeed GOSSELIN adapt to every needs of its users and propose by the way round plates, squares, contact with or without vents. The advantage of GOSSELIN’s Petri Plates is the compatibility with most industrial and non-industrial automatic agar-pouring machines. Petri Plates are manufactured under aseptic conditions according to “clean room technology”.
Perfect Flatness: To ensure the agar’s constant depth
Total Clarity: The injection point situated on the side of the dish bottom of the dish optimizes reading event by image analysing systems
Lightness: Thanks to in-depth research, we have been able to determine the ideal weight of our dishes in order to reduce our customers waste disposal costs while still pursuing our objective: to provide high quality dishes
Stable Stacking: The stacking ring is specially designed to improve the stacking of dishes and making them more practical to use
Class 100 Manufacturing Environment: Ensures dishes are aseptic
Retains Shape up to 55°c: The quality of the polystyrene used provides dishes with a high level of mechanical resistance
Product Traceability: Thanks to the product label on each box, we can retrace each production cycle. This label includes the lot number and if the product has been sterilized, the expiration date
Raw Materials: Compliant with the European directives in force, especially the absence of heavy metals (CE N° 1935/2004), food compatibility (94/62/EC) and CE marking relating to medical devices for invitro diagnostics (98/79/EC)