Data / Medical devices / Germany / Weinmann Emergency Medical Technology GMBH
Weinmann Emergency Medical Technology GMBH: FDA-registered device maker in Hamburg, Germany, 1 510(k) clearance
Weinmann Emergency Medical Technology GMBH is registered with the FDA (registration 3017365972) in Hamburg, Germany. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 20, 2020. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3017365972
- Address
- Frohboesestrasse 12, Hamburg, Germany, 22525
- Owner or operator
- WEINMANN Emergency Medical Technology GmbH (10059708)
- Roles
- Manufacturer
- First device listed
- December 1, 2020
- Registered through
- 2026
- Brand names listed
- MEDUMAT Easy CPR
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Ventilator, Emergency, Powered (Resuscitator) | BTL | 2 | Manufacturer | accessdata.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.
| Decided | 510(k) number | Device | Product code | Decision | Applicant | Source |
|---|---|---|---|---|---|---|
| November 20, 2020 | K193191 | MEDUMAT Easy CPR, MEDUMAT Easy CPR with bag | BTL | Substantially Equivalent | Weinmann Emergency Medical Technology GmbH + Co. KG | accessdata.fda.gov |
Compare with other makers
Updated November 20, 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.