SLEE medical GmbH
Germany Last updated 25 Oct 2026
- Devices
- 15
- Registries
- EUDAMEDFDA
- FDA recalls
- 0
Catalogue
Cut 6062 Ref 10080001
Cut 5062 Ref 10070001
Mtp Ref 11000200
Cut 4062 Ref 10065000
Cellutec Pro + Ref 11000710
Staintec Mini Ref 17005000
Trimtec Ref 10190001
Cellutec Pro Ref 11000700
Mps P2 Ref 10185000
Paraffin Wax Embedding Centre MPS P1 Ref 10190000
Covertec Ref 19000000
Mps P Ref 10170000
Mps C Ref 10175000
Mps W Ref 10180000
Mps Cx Ref 10175020
Frequently asked questions
How many devices does SLEE medical GmbH have in the registry?
The registry currently lists 15 devices for SLEE medical GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list SLEE medical GmbH's devices?
Among its 15 most recently registered devices, SLEE medical GmbH has devices listed in EUDAMED (15 devices).
What risk classes do SLEE medical GmbH's devices fall under?
Among its 15 most recently registered devices, the classes recorded for SLEE medical GmbH's devices are IVDR Class A. Each device page shows its own class and authorisation.
What are the newest devices from SLEE medical GmbH in the registry?
The most recently registered devices listed for SLEE medical GmbH include CUT 6062, CUT 5062, MTP and CUT 4062.
Information
- Address
- 14, Am Neuberg, Nieder-Olm, Germany
- Website
- slee.de
- [email protected]
- PRRC contact
- Alexander Schaumburg
- EUDAMED SRN
- DE-MF-000041949
- FDA FEI number
- 3008399755