Statistics for Hammtek

1Total Devices

1Basic UDI-DIs

0Not destined for EU market

0Certificates

0Valid

0Expiring < 6 months

1Countries

Certificate health for Hammtek

No certificates registered for this manufacturer.

Showing 1–1 of 1 devices.

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
HammTek-Business	`HammTek-Business`	`64298114990012`	1	On the market

Devices placed in 1 country

MD Atlas update: May 27, 2026

FI-MF-000033354

Active

Name: Finnish Medicines Agency, Supervision and licences, Medical Device Unit
SRN: FI-CA-006
Phone: +358 29 522 3341
Email: registry@fimea.fi

NADERI Sanaz
• Led product team of Hammtek for regulatory product compliance on product. • Adhered to state requirements for Fimea, European Database on Medical Devices registrations. • Managed all regulatory needs for product such as EMC (IEC 60601-1-2:2014), risk management (EN ISO 14971:2019), user usability (IEC 62366-1:2015), clinical investigations, clinical evaluation, and labeling (EN ISO 15223-1:2016).
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