Skip to content

Devices Categories Manufacturers Importers Certifiers Authorities Reps. Representatives

Results for “Articulator 00711807”

Name, manufacturer or identifier

Manufacturer (optional)

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 Verified only

Category (EMDN)

Browse by category

3 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

Status

Regime

Registry

Class

Articulator 00711807 UDI-DI 10724995180857

US Endoscopy,FDA registration: United States

None Registry: GUDID Class:II
2 variants
- Articulator 00711807 00711807 Withdrawn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

Active Regimes: 510(k) Registry: 510(k) Class:II

Previous Next

Showing 1-3 of 3

deviCERTS Global Medical Device Regulatory Database

About [email protected]

© 2026 deviCERTS — digitaly.site