V. Guldmann A/S
DK Last updated 23 Oct 2026
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- Devices
- 0
- Registries
- FDA
- FDA recalls
- 0
Catalogue
No devices listed yet from this manufacturer.
Information
- Country
- DK
- Address
- GRAHAM BELLS VEJ 23 A, AARHUS N Midtjylland
- Website
- www.guldmann.com
- FDA FEI number
- 3002835648