MT.DERM GmbH
Active in EUDAMEDGermanyfrom SRN EUDAMED FDA SRN DE-MF-000005784 FEI 3006634874
- Devices
- 9
- Registrations
- EUDAMEDFDA
- FDA recalls
- 0
At a glance
EU certificates
1 of 1 in force.
Market reach
- European Union
- EUDAMED actor, 1 certificate
- United States
- FDA FEI
Catalogue
6-MNP 1.5 ToskaniMED EU Ref EMNPA4806EUMP
Regimes: CE MDR Registry: EUDAMEDExceed Unlimited Ref CG100206MP
Regimes: CE MDR Registry: EUDAMED6-MNP 1.5 Exceed Ref EMNPAED06MP
Regimes: CE MDR Registry: EUDAMED- Regimes: CE MDR Registry: EUDAMED
6-MNP 1.5 Exceed II 3.0 Ref EMNPEY06MP
Regimes: CE MDR Registry: EUDAMEDExceed Ref AD61MP
Regimes: CE MDR Registry: EUDAMEDExceed Microneedling Device Ref K180778
Regimes: 510(k) Registry: 510(k)Exceed Microneedling device Ref K182407
Regimes: 510(k) Registry: 510(k)Exceed Unlimited Ref K233709
Regimes: 510(k) Registry: 510(k)
Company details
- EUDAMED SRN
- DE-MF-000005784
- FDA FEI number
- 3006634874
- EU VAT number
- DE 812 717 153
- EUDAMED status
- Active
- EUDAMED registered name
- MT.DERM GmbH
- Registered address
- 37 - 61, Blohmstraße, 12307, Berlin, Germany
- Website
- www.mtderm.de
- [email protected]
- Phone
- +49 30 76 766 220 0
- PRRC contact
- Dr. Jan Tentrop
EUDAMED certificates
1 certificate1 valid, 0 expiredMDR 1next expiry 23 Jan 2030
TÜV SÜD Product Service GmbH 0123 1 certificate
- G10 067752 0020 Active
Quality management system EU MDR
- Issued
- 24 Jan 2025
- Expires
- 23 Jan 2030
From the company website
MT.DERM is the market leader for cosmetics in the field of piercing substances into the skin. In addition to the cosmetic application and the development of innovative tattoo equipment, we are also very successful as a medical technology company in the medical application.
Frequently asked questions
How many devices does MT.DERM GmbH have in the registry?
The registry currently lists 9 devices for MT.DERM GmbH. Devices recorded under merged duplicate company entries are counted once.
Which registries list MT.DERM GmbH's devices?
Among its 9 most recently registered devices, MT.DERM GmbH has devices listed in EUDAMED (6 devices) and FDA 510(k) (3 devices). A device can be listed in more than one registry, so these counts overlap.
What risk classes do MT.DERM GmbH's devices fall under?
Among its 9 most recently registered devices, the classes recorded for MT.DERM GmbH's devices are Class IIa and Class II. Each device page shows its own class and authorisation.
What EUDAMED certificates are recorded for MT.DERM GmbH?
EUDAMED lists 1 certificate for MT.DERM GmbH (quality management system) under MDR. 1 is recorded with the status issued. The most recent was issued on 24 Jan 2025.
What are the newest devices from MT.DERM GmbH in the registry?
The most recently registered devices listed for MT.DERM GmbH include 6-MNP 1.5 ToskaniMED EU, Exceed Unlimited, 6-MNP 1.5 Exceed and ToskaniMED.