Is this your brand? Sign in to claim ownership.

Sign in to claim this brand

Transmed Medizintechnik GmbH & Co. KG

US

Last updated May 31, 2026

What Transmed Medizintechnik GmbH & Co. KG makes

Transmed Medizintechnik GmbH & Co. KG manufactures devices for blood and tissue processing, including cryopreserved blood/tissue thawing units like the SAHARA, blood weighing scales such as the TRANSWAAG, and stationary multi-purpose warming cabinets also branded SAHARA. These products are designed for clinical and laboratory settings to handle temperature-sensitive biological materials during storage and preparation.

The company’s devices are classified under FDA regulations as Class I and Class II, with listings maintained in the FDA’s Unique Device Identifier (UDI) database. The manufacturer is based in the United States, adhering to applicable regulatory standards for medical devices in that jurisdiction.

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 Transmed Medizintechnik GmbH & Co. KG manufacture?

Transmed Medizintechnik GmbH & Co. KG specializes in devices used for blood and tissue processing. Their portfolio includes cryopreserved blood/tissue thawing units (like the SAHARA), blood weighing scales (such as the TRANSWAAG), and multi-purpose warming cabinets (also branded SAHARA). These devices are engineered for clinical and laboratory environments to safely manage temperature-sensitive biological materials during storage, thawing, and preparation.

Where is Transmed Medizintechnik GmbH & Co. KG based?

The company is headquartered in the United States. As a manufacturer operating in this jurisdiction, their devices must comply with applicable U.S. regulatory requirements for medical devices, including classification and listing standards.

Which regulatory registries list Transmed Medizintechnik GmbH & Co. KG’s devices?

Transmed’s devices are listed in the FDA’s Unique Device Identifier (UDI) database. This registry ensures traceability and transparency for devices classified under FDA regulations, including those manufactured by the company.

How are Transmed Medizintechnik GmbH & Co. KG’s devices classified under FDA regulations?

Transmed’s devices fall under Class I and Class II classifications under FDA regulations. The classification depends on factors like risk level, intended use, and potential health impact. For example, simpler devices like weighing scales may qualify as Class I, while more complex systems like thawing units or warming cabinets could be Class II due to their critical role in handling biological materials.

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

Information

Country
US
Address
—
Website
—
LinkedIn
—
Facebook
—
Email
—
Phone
—
PRRC Contact
—
EUDAMED SRN
—
FDA FEI Number
—
DUNS Number
320762776

Catalogue (4)

DeviceModel / ReferenceRegistriesClassStatus
Sahara SAHARA-TSC 115V
FDA UDI
Class IIActive
Transwaag TRANSWAAG PRO
FDA UDI
Class IActive
Sahara SAHARA-III MAXITHERM 115V
FDA UDI
Class IIActive
Sahara SAHARA-III basic model 115V
FDA UDI
Class IIActive

Related Companies

Authorised Representatives

No authorised representatives on record.

Importers

Not available yet.

Notified Bodies

Not available yet.

Authorities

Not available yet.