Skip to content
devi
CERTS
Devices
Categories
Manufacturers
Importers
Certifiers
Authorities
Reps.
Representatives
Results for “”
Name, manufacturer or identifier
Search
Manufacturer
(optional)
Filters
1 active
Filters
1 active
Registry
EUDAMED
FDA 510(k) incl. De Novo
FDA PMA
GUDID
18
Country / market
United States
18
Risk class
Class I
Class IIa
Class IIb
Class III
18
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
Reset
18 devices found
·
sorted by relevance
Key
Manufacturer: Medtronic 3F Therapeutics, Inc.
×
Clear all
Device
Device · Manufacturer · Authorizations
Verified
Verified
Status
Status
Regime
Regime
Registry
Registry
Class
Class
3f® 1000-21
Medtronic 3F Therapeutics, Inc.
·
,
FDA registration: United States
Group of variants
GUDID
not on market
Withdrawn
Registry:
GUDID
Class
Class:
III
3f® 1000-29
Medtronic 3F Therapeutics, Inc.
·
,
FDA registration: United States
Group of variants
GUDID
not on market
Withdrawn
Registry:
GUDID
Class
Class:
III
3f® 1000-23
Medtronic 3F Therapeutics, Inc.
·
,
FDA registration: United States
Group of variants
GUDID
not on market
Withdrawn
Registry:
GUDID
Class
Class:
III
3f® 1000-25
Medtronic 3F Therapeutics, Inc.
·
,
FDA registration: United States
Group of variants
GUDID
not on market
Withdrawn
Registry:
GUDID
Class
Class:
III
3f® 1000-27
Medtronic 3F Therapeutics, Inc.
·
,
FDA registration: United States
Group of variants
GUDID
not on market
Withdrawn
Registry:
GUDID
Class
Class:
III
Previous
Next
Showing 1-18 of 18