We would like to draw your attention towards The BIRR Labware collection because they are designed in close collaboration with embryologists and produced in the EU, according to the highest quality standards. The entire Labware portfolio is of course CE Class IIa MDD certified. Selected products have The smART Labware Label which indicates innovative features and added value on ease of use or safety compared to conventional labware.
The BIRR Labware collection
The dishes are specifically designed for IVF and all manufactured by BIRR in EU. The dishes are characterized by the following features:
- Class IIa sterile Medical Device in accordance with the 93/42 EEC Directive
- Sterility assurance level 10^6 (by irradiation)
- Raised bottoms (200 micron air layer) to avoid scratches, minimize overheating in case of temperature spikes in the heated stage and provide even adherence to the surface
- Scratch protection improves visibility and safety
- Temperature consistency across all dishware suite
BIRR also offers IVF tubes, IVF pipettes and IVF containers and to receive a complete catalog with The BIRR Labware collection, please contact us at firstname.lastname@example.org.
BIRR is a family-owned Netherlands-based company and specializes in the supply of products for use in Assisted Reproductive Technologies (ART). Their portfolio contains a broad range of products, including a broad IVF Labware portfolio and ART procedure sets.
Dedication and agility
BIRR has a long history of collaboration with hospitals and clinics throughout the world. The company develops, manufactures and sells disposable ART supplies. Their in-depth knowledge and experience enables them to cover the whole process from analysis through to treatment. This has resulted in a broad product range from high quality sperm counting chambers to customized disposable procedural trays for Oocyte Pick up, ET and IUI treatments.
Their research department, advised by IVF pioneer Dr. Jan Vermeiden, brings a wealth of experience in the field of fertility.
All manufactured medical devices are compliant to applicable standards and regulations, the organization is certified against 13485:2016, devices hold a CE-mark in accordance with MDD 92/43 EEC.