Skip to content

Devices Categories Manufacturers Importers Certifiers Authorities Reps. Representatives

Results for “IPERESTENSORE A TRE PUNTI”

Name, manufacturer or identifier

Manufacturer (optional)

Filters

Registry EUDAMED 85 FDA 510(k) FDA PMA GUDID

Country / market European Union (all) 85

More countries (1)

Italy 85

Risk class Class I 85 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 Verified only

Category (EMDN)

Browse by category

85 devices foundsorted by relevance

DeviceDevice · Manufacturer · Authorizations Verified

Status

Regime

Registry

Class

Iperestensore a tre punti basculante UDI-DI 08055965370240

G.L.O. SRL,Italy

Active Regimes: CE MDR Registry: EUDAMED Class:I
8 variants
- Iperestensore a tre punti basculante AZP 140 basso, mis.L
- Iperestensore a tre punti basculante AZP 140 basso, mis.XL
- Iperestensore a tre punti basculante AZP 140, mis.L
- Iperestensore a tre punti basculante AZP 140, mis.S
- See all variants of this device

Showing 81-85 of 85

deviCERTS Global Medical Device Regulatory Database

About [email protected]

© 2026 deviCERTS — digitaly.site