| UDI-DI | 06975473970829 |
|---|---|
| Secondary DI | |
| Nr katalogowy | 030010001 |
| Status rynkowy | Na rynku UE |
| Pierwsze wprowadzenie | Malta |
| Wersja EUDAMED | 1 |
| Rodzaj (EMDN) | IVD GENERIC USE CONSUMABLES › SAMPLES COLLECTION DEVICES › BLOOD COLLECTION DEVICES › VENOUS OR ARTERIOUS BLOOD COLLECTION DEVICES › BLOOD COLLECTION, TUBES › BLOOD COLLECTION, TUBES WITH ADDITIVES OR SERUM SEPARATOR; IVD GENERIC USE CONSUMABLES › SAMPLES COLLECTION DEVICES › BLOOD COLLECTION DEVICES › VENOUS OR ARTERIOUS BLOOD COLLECTION DEVICES › BLOOD COLLECTION, TUBES › BLOOD COLLECTION, TUBES WITHOUT ADDITIVES OR SERUM SEPARATOR |
| Kody EMDN | W050101010201 BLOOD COLLECTION, TUBES WITH ADDITIVES OR SERUM SEPARATOR W050101010202 BLOOD COLLECTION, TUBES WITHOUT ADDITIVES OR SERUM SEPARATOR |
Blood Collection Tube
Changsha Renji Medical Equipment Co., Ltd. · CN-MF-000030318
| Basic UDI-DI | 697547397030010001YC |
|---|---|
| Nazwa wyrobu | Blood Collection Tube |
| Model | No Additive, Plain Tube, Clot Activator, Gel & Clot Activator, EDTA K2, EDTA K3, EDTA & Gel, Sodium Citrate 9NC, ESR 4NC, Sodium Citrate & Gel, NaF & EDTA, Lithium Heparin, Sodium Heparin, Lithium Heparin & Gel, Sodium Heparin & Gel, ACD, ACD & Gel |
| Klasa ryzyka | Klasa A |
| Podstawa prawna | IVDR |
| Typ | |
| Użytek profesjonalny | tak |
Brak Danych dodatkowych – dane z backendu interfejsu EUDAMED nie zostały jeszcze pobrane.