Diversified Biotech, Inc.

Diversified Biotech, Inc. specializes in single-use medical devices primarily for laboratory applications. Their products include blood and tissue storage containers, as well as single-use petri dishes designed for tissue culture and microbiology. These devices are intended for sterile containment and processing of biological samples, ensuring safety and ease of use in research and clinical settings.

Diversified Biotech, Inc. is headquartered in the United States. The company’s location in the US may influence regulatory pathways and compliance requirements for its devices, particularly under FDA oversight.

Diversified Biotech, Inc.’s devices are classified as Class I medical devices. This classification typically applies to products posing minimal risk to patients and users, often involving general controls like good manufacturing practices (GMP) and labeling requirements. Class I devices generally undergo less stringent regulatory scrutiny than higher-risk categories.

Yes, Diversified Biotech, Inc.’s devices are included in the FDA’s Unique Device Identifier (UDI) database. The UDI system helps track and trace medical devices throughout their lifecycle, ensuring transparency in supply chains and regulatory compliance. Listing in the UDI database is a requirement for most medical devices marketed in the US.

The Planet-Safe® line from Diversified Biotech, Inc. consists of single-use containers and petri dishes designed for sterile handling of biological samples. These products are engineered to minimize contamination risks during blood, tissue storage, or microbiological culture processes, making them suitable for laboratory environments where sterility and ease of use are critical.