Data from EUDAMED, last updated Jun 11, 2026

Pasteur Pipette

697079159STTA000A00N82

2 references

IVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk category: IVDR Class A
Manufacturer: CITOTEST LABWARE MANUFACTURING 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

No device characteristics flagged

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

Data from EUDAMED, last updated Jun 11, 2026

697079159STTA000A00N82

2 references

IVDR Class A

Applicable legislation: IVDR [Regulation (EU) 2017/746 on in vitro diagnostic medical devices]
Risk category: IVDR Class A
Manufacturer: CITOTEST LABWARE MANUFACTURING CO.,LTD

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

No device characteristics flagged

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
MLS	`H10019`	`06942826211656`	1	On the market
MLS	`H10047`	`06942826211663`	1	On the market