Data / Medical devices / Spain / International Emergency Services S.L
International Emergency Services S.L: FDA-registered device maker in Derio Bizkaia Vizcaya, Spain, 1 510(k) clearance
International Emergency Services S.L is registered with the FDA (registration 3031754300) in Derio Bizkaia Vizcaya, Spain. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated March 26, 2014. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3031754300
- Address
- Bizkaia Science and Technology Park, Ibaizabal bidea, 500, Derio Bizkaia Vizcaya, Spain, E-48160
- Owner or operator
- International Emergency Services S.L (10091148)
- Roles
- Manufacturer
- First device listed
- July 12, 2024
- Registered through
- 2026
- Brand names listed
- Cricath, Evone, Tritube, Ventinova, Ventrain
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 |
|---|---|---|---|---|---|---|
| March 26, 2014 | K132759 | VENTRAIN | BTL | Substantially Equivalent | Dolphys Medical B.V. | accessdata.fda.gov |
Compare with other makers
Updated March 26, 2014. 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.