Coffalyser.Net

MRC Holland B.V. · NL-MF-000000437

Wariant (UDI-DI)
UDI-DI08720211482816
Secondary DI
Nr katalogowyCoffalyser.Net
Status rynkowyNa rynku UE
Pierwsze wprowadzenieHolandia
Wersja EUDAMED1
Rodzaj (EMDN)REAGENTS › GENETIC TESTING › INBORN GENE OR CHROMOSOME ALTERATIONS › MONOGENETIC DISORDERS › CYSTIC FIBROSIS; REAGENTS › GENETIC TESTING › INBORN GENE OR CHROMOSOME ALTERATIONS › MONOGENETIC DISORDERS › DUCHENNE MUSCULAR DYSTROPHY; REAGENTS › GENETIC TESTING › INBORN GENE OR CHROMOSOME ALTERATIONS › MONOGENETIC DISORDERS › THALASSAEMIA; REAGENTS › GENETIC TESTING › INBORN GENE OR CHROMOSOME ALTERATIONS › MONOGENETIC DISORDERS › MONOGENETIC DISORDERS TESTS - OTHER; REAGENTS › GENETIC TESTING › INBORN GENE OR CHROMOSOME ALTERATIONS › POLYGENETIC DISORDERS › POLYGENETIC DISORDERS TESTS - OTHER; REAGENTS › GENETIC TESTING › INBORN GENE OR CHROMOSOME ALTERATIONS › CHROMOSOMAL DISORDERS › MULTIPLE DETECTION OF CHROMOSOMAL DISORDERS TESTS; REAGENTS › GENETIC TESTING › INBORN GENE OR CHROMOSOME ALTERATIONS › CHROMOSOMAL DISORDERS › CHROMOSOMAL DISORDERS TESTS - OTHER; REAGENTS › GENETIC TESTING › INBORN GENE OR CHROMOSOME ALTERATIONS › POLYMORPHISMS › HLA-TYPING; REAGENTS › GENETIC TESTING › ACQUIRED GENE OR CHROMOSOME ALTERATIONS › TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER
Kody EMDNW0106010101 CYSTIC FIBROSIS
W0106010102 DUCHENNE MUSCULAR DYSTROPHY
W0106010111 THALASSAEMIA
W0106010199 MONOGENETIC DISORDERS TESTS - OTHER
W0106010299 POLYGENETIC DISORDERS TESTS - OTHER
W0106010306 MULTIPLE DETECTION OF CHROMOSOMAL DISORDERS TESTS
W0106010399 CHROMOSOMAL DISORDERS TESTS - OTHER
W0106010401 HLA-TYPING
W01060299 TESTS FOR ACQUIRED GENETIC OR CHROMOSOMAL ALTERATIONS - OTHER
Wyrób (Basic UDI-DI)
Basic UDI-DI872021148Coffalyser.NetVM
Nazwa wyrobuCoffalyser.Net
Model
Klasa ryzykaKlasa A
Podstawa prawnaIVDR
Typ
Użytek profesjonalnytak
Dane dodatkowe

Brak Danych dodatkowych – dane z backendu interfejsu EUDAMED nie zostały jeszcze pobrane.