Skip to the page

Data / Medical devices / Italy / Sidam SRL

Sidam SRL: FDA-registered device maker in Mirandola Modena, Italy, 1 510(k) clearance

Sidam SRL is registered with the FDA (registration 3005441393) in Mirandola Modena, Italy. It lists 2 device types. The FDA files 1 510(k) clearance under its listings, the newest dated July 31, 2020. Registered through 2026. FDA data exported November 2, 2026.

SpecStream is the live web data engine for teams and agents. It reads the FDA registration and listing, 510(k), PMA, recall and enforcement files from openFDA every week, and this page is that reading, joined by the FDA's own numbers. Ask for the makers of any device type in any country and new clearances, approvals and recalls arrive in your sheet, CRM, Slack or agent as the FDA publishes them.

FDA registration number
3005441393
Address
Via Statale Sud, 169, Mirandola Modena, Italy, 41037
Owner or operator
Sidam Srl (10054097)
Roles
Contract manufacturer, Manufacturer
First device listed
September 6, 2018
Registered through
2026
Brand names listed
Cyber Blade, ulrichINJECT CT motion, ulricheasyINJECT Max

Devices it lists

DeviceProduct codeClassRoleSource
Injector, Contrast Medium, AutomaticIZQ2Contract manufactureraccessdata.fda.gov
Laparoscope, General & Plastic SurgeryGCJ2Manufactureraccessdata.fda.gov

510(k) clearances

The 510(k) numbers this establishment lists, with the FDA decision on each. The applicant is the company that holds the clearance.

Decided510(k) numberDeviceProduct codeDecisionApplicantSource
July 31, 2020K192499Cyber BladeGCJSubstantially EquivalentSIDAM S.r.l.accessdata.fda.gov

Compare with other makers

Updated July 31, 2020. Read from openFDA bulk downloads (device registration and listing, 510(k), PMA, recall and enforcement files). CC0 1.0, public domain (openFDA terms of service). The files are joined on FDA identifiers: the 510(k) and PMA numbers a registration lists, and the recalling firm's FEI for recalls. Recall class comes from the FDA enforcement report. The FDA states that openFDA data is unvalidated and is not for decisions about medical care. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.