Results for “Archwire AMC1825LNITI”

Name, manufacturer or identifier

Manufacturer (optional)

Filters

Registry EUDAMED FDA 510(k) FDA PMA GUDID 3

Country / market United States 3

Risk class Class I 3 Class IIa Class IIb Class III 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 Validated only

Category (EMDN)

Browse by category

3 devices foundsorted by relevance

Clear all

Device · Manufacturer · Authorizations

Archwire AMC1825LNITIEU

Acme-Monaco Corp.,FDA registration: United States Class I

None GUDID I
Archwire AMC1825LNITI UDI-DI D972AMC1825LNITI2

Acme-Monaco Corp.,FDA registration: United States Class I

None GUDID I
2 variants
- Archwire AMC1825LNITI AMC1825LNITI

Previous Next

Showing 1-3 of 3

deviCERTS Global Medical Device Regulatory Database

About [email protected]

Results for “Archwire AMC1825LNITI”

Category (EMDN)

Archwire AMC1825LNITIEU

Archwire AMC1825LNITI UDI-DI D972AMC1825LNITI2