Skip to content
devi
CERTS
Devices
Categories
Manufacturers
Importers
Certifiers
Authorities
Reps.
Representatives
Results for “Gentle Max Pro”
Name, manufacturer or identifier
Search
Manufacturer
(optional)
Filters
Filters
Registry
EUDAMED
3
FDA 510(k) incl. De Novo
FDA PMA
GUDID
3
Country / market
European Union (all)
3
United States
3
More countries (1)
Denmark
3
Risk class
Class I
Class IIa
Class IIb
3
Class III
Class II (US)
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
Verified only
Category (EMDN)
Browse by category
Apply filters
3 devices found
·
sorted by relevance
Key
Clear all
Device
Device · Manufacturer · Authorizations
Verified
Verified
Status
Status
Regime
Regime
Registry
Registry
Class
Class
Gentle Max Pro Plus
Candela Corporation
·
,
United States
CE/MDD
GUDID
on market
Active
Regimes:
CE MDD
Registry:
EUDAMED
GUDID
Class
Class:
IIb
Gentle Max Pro
Candela Corporation
·
,
United States
Group of variants
CE/MDD
GUDID
on market
Active
Regimes:
CE MDD
Registry:
EUDAMED
GUDID
Class
Class:
IIb
Previous
Next
Showing 1-3 of 3