Isidakamizwa sokuqala esigunyazwe yi-FDA esenziwe insangu manje esitholakala e-US |Ikhebula le-Ecg lesiguli

Noma kunjalo, kukhona impikiswano mayelana nenani le-ECG ngokwayo.I-US Preventive Task Force incoma ngokumelene nokuhlolwa kwe-ECG kubantu abadala abasengozini ephansi yesifo senhliziyo nemithambo yegazi.Iqembu, elizikhomba “njengephaneli elizimele, lamavolontiya lochwepheshe bakazwelonke kwezokuvikela kanye nemithi esekelwe ebufakazini,” lengeze ngokuthi “abukho ubufakazi obanele” kubantu abadala abasengozini ephakathi noma ephakeme.

Imakethe yomhlaba wonke ye-ECG leadwires ibuswa yiNyakatho Melika ngenxa yokwanda kwesifo sikashukela, ekhuphuka inani leziguli ezihlushwa i-CVD, nokwamukelwa kwempilo yedeskithophu, nokunye.Ngaphezu kwalokho, ukushintsha indlela yokuphila yabantu, ukuba khona kwabaholi bomhlaba wonke abavela ezimakethe kanye nokusetshenziswa kwemali okuphezulu ekwelapheni kukhuthaze ukukhula kwemakethe.I-Europe ikleliswe endaweni yesibili ehamba phambili ilandelwa yi-Asia Pacific.I-Asia Pacific iyimakethe ye-ECG ehamba phambili ekhula ngokushesha ngenxa yokuba khona kwechibi elikhulu leziguli, okwandisa ukwesekwa kukahulumeni kanye nokuba khona kweminotho ethuthuka ngokushesha.I-China ne-India kulindeleke ukuthi ibe nesabelo esivelele emakethe ngenxa yesibalo esikhulu sabantu abanesifo sikashukela kanye nesidingo esiqhubekayo semishini ethuthukisiwe.Ngakolunye uhlangothi, iLatin America, Middle East kanye ne-Afrika (LAMEA) ibamba isabelo esincane emakethe.Yize isifunda sinesabelo esincane kakhulu kodwa maduze nje lokhu kuzovela njengesinye sesifunda esivelele emakethe.

Ucwaningo lubandakanya abashayeli bemakethe, abakhona kanye namathuba okukhula azayo, izinselelo ezihlakaniphile zesigaba kanye nesifunda ezibhekene nemakethe ye-ECG Cable kanye ne-ECG Lead Wires, isimo sokuncintisana emakethe yomhlaba.Isimo sombiko wesifunda sihlanganisa usayizi wemakethe kanye nokuqhathaniswa kwezifunda okuyiNyakatho Melika, iYurophu, i-Asia Pacific (APAC), Middle East kanye ne-Afrika (MEA), kanye neLatin America.

Thola Umbiko Wemakethe Ophelele Wezinto Zokusebenza Zezokwelapha Eziphathekayo @ https://www.360marketupdates.com/purchase/12560974

Ngokwendawo, lo mbiko uhlukaniswe ngezifunda ezibalulekile ezimbalwa, ngokukhiqiza, ukusetshenziswa, imali engenayo (isigidi se-USD), nesabelo semakethe kanye nezinga lokukhula kwe-High Frequency Spindle kulezi zifunda, kusukela ngo-2018 kuya ku-2025 (isibikezelo),

Imibiko yesampula ye-Technavio imahhala futhi iqukethe izigaba eziningi zombiko ezifaka usayizi wemakethe nesibikezelo, abashayeli, izinselele, amathrendi, nokuningi.

I-Cardiac Insight ithe i-Cardea SOLO inganciphisa izinsuku noma amaviki esikhathi sokushintsha umbiko we-ECG uma kuqhathaniswa nokusebenzisa izinsizakalo zokubika ze-ECG zenkampani yangaphandle.Iwukuphela kwe-PC-based PC-based Analysis Software esulwe yi-US Food and Drug Administration (FDA) ukukhiqiza umbiko ozenzakalelayo wesifinyezo esisalungiswa ngaphandle kokungenelela komuntu.Umbiko usulungele ukubuyekezwa kodokotela noma uhlelwe emizuzwini emihlanu noma ngaphansi.I-Cardea SOLO Software futhi inikeza odokotela ukufinyelela, kanye nobunikazi bakho, konke ukushaya kwenhliziyo kwedatha yesiguli ukuze kuhlaziywe okwengeziwe.

I-Global Pulse Oximeter Market: Ukuhlaziywa Kwesigaba Sezicelo Sesikhungo Sokuhlinza Sesikhungo Sokuhlinza Ekhaya

Isicelo se-FDA solwazi olwengeziwe sidinga ukuhlolwa kwangaphandle nokuzimele kwenkampani yangaphandle ukuze kutholwe ukuhambisana kokukhishwa kogesi kagesi nokukhipha ugesi.I-FDA iphinde yacela idatha eqinisekisa ikhono ledivayisi lokuqopha ama-ECG ekhwalithi yomtholampilo elinganayo, uma kuqhathaniswa nama-ECG aqoshwe kusetshenziswa amapheshi kagesi e-ECG avamile namakhebula e-ECG.I-CardioComm inikezwe ubuningi bezinsuku eziyi-180 ukuze iphendule kumhloli we-FDA.Nakuba Inkampani ihlose ukuphendula i-FDA phakathi kwezinsuku ezingu-90, ukuhlolwa okuceliwe kanye nemibhalo evela kwabanye abantu akuzange kuvumele impendulo eya ku-FDA ukuba igcwaliswe phakathi nalesi sikhathi.Konke ukuhlolwa kwedivayisi manje sekuphasisiwe futhi imiphumela yahlanganiswa ukuze kuphendulelwe i-FDA.Iwashi le-Substantive Review lizoqala kabusha uma i-FDA isitholile futhi yamukela impendulo yeNkampani.Ngokusekelwe emigqeni yesikhathi eshicilelwe ye-FDA, Inkampani iphrojekthi yokuphothulwa okungenzeka kokubuyekezwa kwesicelo esingu-510(k) ekupheleni kukaDisemba 2018. Inkampani iphawula ukuthi i-FDA inamandla okucela isikhathi esengeziwe sokuqedela isibuyekezo sayo ngokubona kwe-FDA.

UKyle ungunjiniyela wekhompyutha ngokweziqu kanye nombhali we-cryptocurrency cum blogger ngokomsebenzi.Ngaphandle kwe-pizza nebhola, uyamangala ngobuchwepheshe be-blockchain kanye nokusebenza kwabo.Ngakho-ke ngenxa yesizinda sobuchwepheshe kanye nombhali ochwepheshile, ulingana ngokuphelele.

Kulo mbiko, sengeze isifinyezo esijulile sezinto ezintsha ezikhona, ukucaciswa, ipharamitha, nokukhiqiza.Lo mbiko uhlanganisa indawo enkulu yesifunda enenani lezinhlangano ezidumile, abathengisi, nabakhiqizi.

Ekugcineni, umbiko uhlanganisa amathuba emakethe ye-Medical Cable Assemblies kanye nezici zokuncintisana zabanikazi bamasheya kanye nabaholi bemakethe be-Medical Cable Assemblies.Umbiko we-Medical Cable Assemblies uphinde wethula izinqubo zocwaningo, izinhlelo zokutshala imali, kanye nokuhlaziywa kokuvela kwemboni ye-Medical Cable Assemblies.Ekugcineni, ngosizo locwaningo oluphelele lwemboni ye-Medical Cable Assemblies yenkathi ebikezelayo 2018 kuya ku-2025, ingasiza umuntu ekwenzeni izinqumo zebhizinisi ezingadala ukuzuza ukukhula kwebhizinisi ngokushesha emakethe ye-Medical Cable Assemblies emhlabeni jikelele.