Ntugharị ọgwụ mgbochi dị elu nke nwere ike ịgbanye agịga na-enweghị njikọ njikọta

Ngwunye ọgwụ dị elu nke enwere ike ịgbanye agịga na-enweghị njikọ na-anọpụ iche nke egosipụtara

Nkọwa dị mkpirikpi:

● Sterile, Na-adịghị egbu egbu, Na-abụghị Pyrogenic

● A na-asachapụ ngwa ngwa maka mmetọ dị mma

● Usoro mechiri emechi na-enyere aka ibelata ihe ize ndụ nke ibute ọrịa

● Oghere anwụ dị ala na-ebelata mmepe biofilm

● Kwe ka a na-ahụ anya na-agbapụta mmiri. Belata ihe ize ndụ nke ịchịisi

● A na-eme njikọ agịga n'efu iji belata reflux ọbara, zere oghere catheter. Ụzọ mmiri kwụ ọtọ nke dị n'ime na-enyere aka iwelata ụda priming ma gboo nchegbu oghere nwụrụ anwụ

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Nkọwa ngwaahịa

Mkpado ngwaahịa

Njirimara ngwaahịa

Ezubere iji	A na-eji njikọ njikọ infusion na ngwa infusion ma ọ bụ IV catheter maka intravenous infusion na ọgwụ ọgwụ.
Nhazi na nhazi	Ngwaọrụ ahụ nwere okpu nchebe, plọg rọba, akụkụ dosing na njikọ. Ngwa niile na-egbo mkpa ahụike.
Isi ihe	PCTG+ silicon rọba
Ndụ nchekwa	Afọ ise
Asambodo na Nkwenye Ogo	N'ikwekọ na iwu (EU) 2017/745 nke ndị omebe iwu Europe na nke Council (CE Class: Is) Usoro nrụpụta na-agbaso ụkpụrụ ISO 13485 Quality System.