Data from EUDAMED, last updated Jun 11, 2026

Sample Diluent

6970493090801018PE

2 references

IVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk category: IVDR Class A
Manufacturer: Shenzhen Dymind Biotechnology Co., Ltd.

Device family identification

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk category: IVDR Class A
Status: On the market

ReagentProfessional testing

European Medical Device Nomenclature — the EU product classifications carried across this device family's references.

Data from EUDAMED, last updated Jun 11, 2026

6970493090801018PE

2 references

IVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk category: IVDR Class A
Manufacturer: Shenzhen Dymind Biotechnology Co., Ltd.

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk category: IVDR Class A
Status: On the market

ReagentProfessional testing

European Medical Device Nomenclature — the EU product classifications carried across this device family's references.

2 references

Trade name	Reference / catalog number	UDI-DI code	Quantity	Status
Sample Diluent	`12.02.0804A`	`06976117453265`	25	On the market
Sample Diluent	`12.02.0805A`	`06976117453272`	50	On the market