Skip to content
devi
CERTS
Devices
Categories
Manufacturers
Importers
Certifiers
Authorities
Reps.
Representatives
Results for “AMICA-PROBE”
Name, manufacturer or identifier
Search
Manufacturer
(optional)
Filters
Filters
Registry
EUDAMED
238
FDA 510(k)
1
FDA PMA
GUDID
60
Country / market
European Union (all)
182
United States
61
More countries (1)
Italy
182
Risk class
Class I
Class IIa
Class IIb
183
Class III
Class II (US)
61
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
244 devices found
·
sorted by relevance
Key
Clear all
Device
Device · Manufacturer · Authorizations
Verified
Verified
Status
Status
Regime
Regime
Registry
Registry
Class
Class
Hs Amica Rf Amica-Probe
H.S. Hospital Service SpA
·
,
FDA registration: United States
GUDID
not on market
Withdrawn
Registry:
GUDID
Class
Class:
II
Amica-Gen Agn-H-1.3, Amica-Gen Agn 3.3, Amica-Probe 17g & 18g
H.S. Hospital Service S.p.A.
·
,
Italy
FDA 510(k)
K232072
Active
Cleared 9 Feb 2024
Active
Regimes:
510(k)
Registry:
510(k)
Class
Class:
II
Previous
Next
Showing 241-244 of 244