10,000 results
·
426ms
·
Sources: EU EUDAMED, US FDA
ARi ExCon Implant
FDA UDI
Megagen Implant Co. Ltd·08809931182098·
ARi ExCon Implant
FDA UDI
Megagen Implant Co. Ltd·08809854028763·
ARi ExCon Implant
FDA UDI
Megagen Implant Co. Ltd·08809931182432·
ARi ExCon Implant
FDA UDI
Megagen Implant Co. Ltd·08809931181916·
BIOSTER, a.s.
Manufacturer
🇨🇿 Czechia·INSTITUT PRO TESTOVÁNI A CERTIFIKACI, a. s. (INSTITUTE FOR TESTING AND CERTIFICATION) merged with ex-NB 1390
Flídr medical s.r.o.
Manufacturer
🇨🇿 Czechia·INSTITUT PRO TESTOVÁNI A CERTIFIKACI, a. s. (INSTITUTE FOR TESTING AND CERTIFICATION) merged with ex-NB 1390
KARDI AI Technologies s.r.o.
Manufacturer
🇨🇿 Czechia·INSTITUT PRO TESTOVÁNI A CERTIFIKACI, a. s. (INSTITUTE FOR TESTING AND CERTIFICATION) merged with ex-NB 1390
ICZ.HEA a.s.
Manufacturer
🇨🇿 Czechia·1 Basic UDI-DI·1 Device·INSTITUT PRO TESTOVÁNI A CERTIFIKACI, a. s. (INSTITUTE FOR TESTING AND CERTIFICATION) merged with ex-NB 1390
BATIST Medical Productions s.r.o.
Manufacturer
🇨🇿 Czechia·INSTITUT PRO TESTOVÁNI A CERTIFIKACI, a. s. (INSTITUTE FOR TESTING AND CERTIFICATION) merged with ex-NB 1390
COMPEX, spol. s r.o.
Manufacturer
🇨🇿 Czechia·INSTITUT PRO TESTOVÁNI A CERTIFIKACI, a. s. (INSTITUTE FOR TESTING AND CERTIFICATION) merged with ex-NB 1390
VINAMET CZ s.r.o.
Manufacturer
🇨🇿 Czechia·INSTITUT PRO TESTOVÁNI A CERTIFIKACI, a. s. (INSTITUTE FOR TESTING AND CERTIFICATION) merged with ex-NB 1390
Spatz FGIA Inc.
Manufacturer
🇺🇸 United States·1 Basic UDI-DI·1 Device·INSTITUT PRO TESTOVÁNI A CERTIFIKACI, a. s. (INSTITUTE FOR TESTING AND CERTIFICATION) merged with ex-NB 1390
VERTEX SYSTEM
FDA 510(k)
FDA Class 2
·Cardiovascular
PROCHECK(TM) BLIND PERFORMANCE SPECIMENS
FDA 510(k)
FDA Class 1
·Clinical Toxicology
MYCOAKT M KANSASII CULTURE ID KIT
FDA 510(k)
FDA Class 1
·Microbiology
ARGUS SYSTEM-CONTINUOUS EXPERT CARE NETWORK
FDA 510(k)
FDA Class 2
·Cardiovascular
MYCOAKT M. TUBERCULOSIS CUULTURE ID KIT
FDA 510(k)
FDA Class 1
·Microbiology
ANKYLOS DENTAL IMPLANT SYSTEM
FDA 510(k)
FDA Class 2
·Dental
FRIALIT-2 MH-2 ABUTMENT
FDA 510(k)
FDA Class 2
·Dental
NON-MYDRIATIC FUNDUS CAMERA, MODEL NM-1000
FDA 510(k)
FDA Class 2
·Ophthalmic