Skip to content
devi
CERTS
Devices
Categories
Manufacturers
Importers
Certifiers
Authorities
Reps.
Representatives
Results for “MOTUS PRO”
Name, manufacturer or identifier
Search
Manufacturer
(optional)
Filters
Filters
Registry
EUDAMED
6
FDA 510(k)
1
FDA PMA
GUDID
2
Country / market
European Union (all)
6
United States
3
More countries (1)
Italy
6
Risk class
Class I
Class IIa
Class IIb
6
Class III
Class II (US)
3
More classes (11)
Class A
Class B
Class C
Class D
IVD General
IVD Annex II List A
IVD Annex II List B
IVD for self-testing
Active implantable (AIMDD)
Unclassified (FDA)
Not classified (FDA)
Verified
Validated only
Category (EMDN)
Browse by category
Apply filters
9 devices found
·
sorted by relevance
Key
Clear all
Device · Manufacturer · Authorizations
Verified
Status
Regime
Registry
Class
Motus Pro M130N1
Deka M.E.L.A. SRL
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
Motus Pro Ax M130P1
Deka M.E.L.A. SRL
·
,
FDA registration: United States
Class II
CE/MDD
GUDID
on market
Active
CE MDD
GUDID
II
Motus Pro
UDI-DI 08034108512761
Deka M.E.L.A. SRL
·
,
Italy
Class IIb
CE/MDD
Active
CE MDD
EUDAMED
IIb
6 variants
Motus Pro
M130H1
Motus Pro
M130I1
Motus Pro
M130K1
Motus Pro
M130L1
Motus Pro
M130M1
MOTUS PRO Family
El.En S.P.A.
·
,
FDA registration: United States
Class II
FDA 510(k)
K241459
Active
Cleared 21 Jun 2024
Active
510(k)
510(k)
II
Previous
Next
Showing 1-9 of 9