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Hamilton AG

Switzerland CH-MF-000013585 Last updated 17 Sep 2026

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Devices
73
Registries
EUDAMED
FDA recalls
0

Catalogue73

Page 2 of 2

Showing 51-77 of 73

EUDAMED certificates1

Held under this manufacturer's EUDAMED registration, grouped by notified body; in force first, then by expiry.

EUDAMED certificates (1)

TÜV Rheinland LGA Products GmbH 0197 1 certificate

  • HX 1774385-1 Amended

    Quality management system EU IVDR

    Issued
    16 Oct 2026
    Expires
    15 Sep 2029
    Reason
    Mnf data change

About

Discover how Hamilton Company supports scientific innovation through engineered solutions, global service, and trusted partnerships. For over 70 years, we’ve helped researchers solve real-world challenges in the lab, in the field, and in production.

From the manufacturer's own website. Source

What Hamilton AG makes

The company manufactures sterile and non-sterile pipette tips, including conductive and standard variants, for laboratory use. It also produces deep well plates, reagent containers, and automated liquid handling systems, such as the ML STARlet IVD-R. The portfolio includes consumables for precise liquid dispensing and sample processing in research and diagnostics.

These devices are classified under Class A per EU regulations and are listed in the EUDAMED database. The company is based in Switzerland.

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 Hamilton AG manufacture?

Hamilton AG produces a range of laboratory consumables and automated systems, primarily focused on pipette tips (both sterile and non-sterile, including conductive variants) and deep well plates. It also offers reagent containers and liquid handling devices like the ML STARlet IVD-R, designed for precise liquid dispensing and sample processing in research and diagnostics.

Where is Hamilton AG based?

Hamilton AG is headquartered in Switzerland, operating from a base in the country. The Swiss location aligns with its focus on precision engineering and compliance with European regulatory standards.

Which regulatory registries list Hamilton AG’s devices?

Hamilton AG’s devices are listed in the EUDAMED database, which is the European Union’s centralised registry for medical devices. This inclusion reflects compliance with EU regulatory requirements for traceability and transparency.

How are Hamilton AG’s devices classified under EU regulations?

Hamilton AG’s devices fall under Class A classification per EU regulations. This classification applies to low-risk products like pipette tips, reagent containers, and certain consumables, where the risk to patients is minimal and the devices are intended for non-invasive use or simple diagnostic procedures.

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

Information

Country
Switzerland
Address
8, Via Crusch, Bonaduz, Switzerland
PRRC contact
Anja Bolli
EUDAMED SRN
CH-MF-000013585