Data / Medical devices / Netherlands / Mauser Benelux B.V.
Mauser Benelux B.V.: FDA-registered device maker in Oosterhout Noord-Brabant, Netherlands, 1 510(k) clearance
Mauser Benelux B.V. is registered with the FDA (registration 3014255019) in Oosterhout Noord-Brabant, Netherlands. It lists 1 device type. The FDA files 1 510(k) clearance under its listings, the newest dated November 1, 2017. Registered through 2026. FDA data exported November 2, 2026.
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- FDA registration number
- 3014255019
- Address
- Souvereinstraat 1, Oosterhout Noord-Brabant, Netherlands, 4903RH
- Owner or operator
- MAUSER Benelux B.V. (10056535)
- Roles
- Manufacturer
- First device listed
- December 19, 2017
- Registered through
- 2026
- Brand names listed
- MAUSER PGII Sharps Container
Devices it lists
| Device | Product code | Class | Role | Source |
|---|---|---|---|---|
| Container, Sharps | MMK | 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 1, 2017 | K170513 | MAUSER PG II Sharps Container | MMK | Substantially Equivalent | Mauzer USA, LLC | accessdata.fda.gov |
Compare with other makers
Updated November 1, 2017. 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.