TarCET PGT incl. WGA

MEDICOVER GENETICS LIMITED · CY-MF-000009381

Wariant (UDI-DI)
UDI-DI05298004820105
Secondary DI
Nr katalogowyET302-00-2016
Status rynkowyNa rynku UE
Pierwsze wprowadzenieCypr
Wersja EUDAMED1
Rodzaj (EMDN)REAGENTS › GENETIC TESTING › INBORN GENE OR CHROMOSOME ALTERATIONS › CHROMOSOMAL DISORDERS › DOWN'S SYNDROME; REAGENTS › GENETIC TESTING › INBORN GENE OR CHROMOSOME ALTERATIONS › CHROMOSOMAL DISORDERS › EDWARDS SYNDROME; REAGENTS › GENETIC TESTING › INBORN GENE OR CHROMOSOME ALTERATIONS › CHROMOSOMAL DISORDERS › KLINEFELTER SYNDROME; REAGENTS › GENETIC TESTING › INBORN GENE OR CHROMOSOME ALTERATIONS › CHROMOSOMAL DISORDERS › PÄTAU SYNDROME; REAGENTS › GENETIC TESTING › INBORN GENE OR CHROMOSOME ALTERATIONS › CHROMOSOMAL DISORDERS › TURNER SYNDROME; REAGENTS › GENETIC TESTING › INBORN GENE OR CHROMOSOME ALTERATIONS › CHROMOSOMAL DISORDERS › CHROMOSOMAL DISORDERS TESTS - OTHER; REAGENTS › GENETIC TESTING › GENETIC TESTS - OTHER
Kody EMDNW0106010301 DOWN'S SYNDROME
W0106010302 EDWARDS SYNDROME
W0106010303 KLINEFELTER SYNDROME
W0106010304 PÄTAU SYNDROME
W0106010305 TURNER SYNDROME
W0106010399 CHROMOSOMAL DISORDERS TESTS - OTHER
W010699 GENETIC TESTS - OTHER
Wyrób (Basic UDI-DI)
Basic UDI-DI52980048PGTZB
Nazwa wyrobuTarCET PGT
Model
Klasa ryzykaKlasa C
Podstawa prawnaIVDR
Typodczynnik, zestaw
Użytek profesjonalnytak
Dane dodatkowe

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

Inne Warianty tego Wyrobu