Results for “2-Way 100% Silicone Cleartract Catheter”

Name, manufacturer or identifier

Manufacturer (optional)

Filters

Registry EUDAMED FDA 510(k) incl. De Novo 3 FDA PMA GUDID

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

Clear all

DeviceDevice · Manufacturer · Authorizations Verified

Status

Regime

Registry

Class

2-Way 100% Silicone ClearTract Catheter

Silq Technologies Corporation,FDA registration: United States Group of variants

Active Regimes: 510(k) Registry: 510(k) Class:II
2-Way 100% Silicone Cleartract Catheter

Silq Technologies, Corp.,United States(FDA applicant)

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]

Results for “2-Way 100% Silicone Cleartract Catheter”

Category (EMDN)

2-Way 100% Silicone ClearTract Catheter

2-Way 100% Silicone Cleartract Catheter