Skip to content
devi
CERTS
Devices
Categories
Manufacturers
Importers
Certifiers
Authorities
Reps.
Representatives
Results for “Articulator 00711810”
Name, manufacturer or identifier
Search
Manufacturer
(optional)
Filters
Filters
Registry
EUDAMED
FDA 510(k)
1
FDA PMA
GUDID
2
Country / market
United States
3
Risk class
Class I
Class IIa
Class IIb
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
3 devices found
·
sorted by relevance
Key
Clear all
Device · Manufacturer · Authorizations
Verified
Status
Regime
Registry
Class
Articulator 00711810
UDI-DI 10724995180871
US Endoscopy
·
,
FDA registration: United States
Class II
GUDID
on market
None
GUDID
II
2 variants
Articulator 00711810
00711810
Withdrawn
Articulator Injection Needle (00711807), Articulator Injection Needle (00711810), Articulator Injection Needle - enteroscope (00711808), Carr-Locke Injection Needle (00711811), Carr-Locke Injection Needle (00711812), Carr-Locke Injection Needle (00711813), Carr-Locke Injection Needle (00711814), Carr-Locke Injection Needle (00711822), Carr-Locke Injection Needle (00711823), Carr-Locke Injection Needle (00711824)
Steris
·
,
FDA registration: United States
Class II
FDA 510(k)
K232826
Active
Cleared 8 Mar 2024
Active
510(k)
510(k)
II
Previous
Next
Showing 1-3 of 3