Numares AG
Germany DE-MF-000022282 Last updated 23 Oct 2026
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- Devices
- 10
- Registries
- EUDAMEDFDA 510(k)FDA
- FDA recalls
- 0
Catalogue
AXINON® System Ref AX0700
AXINON® Sample Wizard Ref AX0403
AXINON® serum kit 2.0 for 100 tests Ref AX0315-100
AXINON® serum kit 2.0 for 500 tests Ref AX0315-500
AXINON® Software Ref AX0402
AXINON® lipoFIT® Ref AX0012
AXINON® serum kit 2.0 for 20 tests Ref AX0315-20
AXINON® serum kit 2.0 for 1000 tests Ref AX0315-1000
Axinon® Gfr(Nmr) Ref AX0028
AXINON® LDL-p Test System Ref K210801
What Numares AG makes
Numares AG manufactures the AXINON® LDL-p Test System, which is a medical device used for testing low-density lipoprotein particle levels.
The AXINON® LDL-p Test System is classified as Class I and is listed in the FDA 510(k) registry. Numares AG is based in the US.
Frequently asked questions
What medical devices does Numares AG manufacture?
Numares AG manufactures the AXINON® LDL-p Test System, which is a medical device used for testing low-density lipoprotein particle levels.
Where is Numares AG based?
Numares AG is based in the US, as indicated in the provided device data.
Which regulatory registries list Numares AG's devices?
Numares AG's devices are listed in the FDA 510(k) registry, as specified in the device data for the AXINON® LDL-p Test System.
How are Numares AG's devices classified?
Numares AG's AXINON® LDL-p Test System is classified as Class I, which is the lowest risk category for medical devices, as indicated in the provided information.
Information
- Country
- Germany
- Address
- 13, Am BioPark , Regensburg, Germany
- Website
- numares.com
- [email protected]
- Phone
- 094128094900
- PRRC contact
- Lutz Niggl
- EUDAMED SRN
- DE-MF-000022282
- FDA FEI number
- 3011080315