*Plura de producto cognoscendi causa, vide infra vel nobis directe scribe.
INFORMATIONES DE ORDINENumerus OEM | |
Fabricator | Numerus Partis OEM |
Mindray > Datascope | 115-020768-00, 040-000332-00, 582A |
Compatibilitas: | |
Fabricator | Modellum |
Edan | Elite V5, Elite V6, Elite V8, iM20, iT20 |
Mindray > Datascope | Accutorr 3, Accutorr 7, BeneView T1, BeneView T5, Benevisio T8, Benevisio N1, Benevisio N12, Benevisio N15, Benevisio N17, Benevisio N19, Benevisio N22, Beneheart D6, DPM6, DPM7, MEC 12, MPM, PM 6800, Congue 12, Congue 12m, Congue VS 8A, VS Congue N19, Benevisio N22, Beneheart D6, DPM6, DPM7, MEC 12, MPM, PM 6800, Congue 12, Congue 12, VS 8C, VS Congue 17m, Congue 8, VS, VS N22, Congue D6, DPM6, DPM7, MEC 12, MPM, PM 6800, Congue 12, Congue 12m, Congue N17, VS Congue N19, Benevisio N22, Beneheart D6, DPM6, DPM7, MEC 12, MPM, PM 6800, Congue 12, Congue 12, VS 8C, VS Congue N17, VS Congue 8A, VS 9C, cPM 12, cPM 8, ePM 10A, ePM 10M, ePM 12, ePM 12M, iMEC 10, iMEC 12, iMEC 15, iMEC 15S, iMEC 5, iMEC 6, iMEC 7, iMEC 8; Series iMEC, iPM 10, iPM 12, iPM 5, iPM 6, iPM 7, iPM 8, Series iPM, iPM-9800 Vide Minus |
Penlon InterMed | Omnes |
Specificationes Technicae: | |
Categoria | Funes Adaptatores SpO2 |
Obsequium regularum | FDA, CE, ISO 80601-2-61:2011, ISO 10993-1, 5, 10:2003E, TUV, RoHS obsequens. |
Coniunctor Instrumentorum | Conector rotundus, masculus, octo-clavorum, clavatus |
Coniunctor Iugi (Latere Sensoris) | Conector D-Sub Femina 9-Clavium, Clavis Triplicis |
Technologia Spo2 | Technicus Masimo LNCS. |
Magnitudo Patientis | Adultus, Paediatricus, Infans, Neonatus |
Longitudo Funis Totalis (pedes) | 7.8 pedes (2.43 m) |
Color Funis | Cinereus |
Diametros Funis | 5.0mm |
Materia Funis | PVC |
Sine latex | Ita |
Typus Involucri | Saccus |
Unitas Involucri | 1 pecia |
Pondus Sarcinae | 110g |
Garantia | / |
Sterilis | NO |
*Declaratio: Omnia signa mercatoria, nomina, exempla, etc., in contento supra demonstrata, ad possessorem originalem vel fabricatorem originalem pertinent. Hic articulus solum ad demonstrandam compatibilitatem productorum MedLinket adhibetur. Nulla alia intentio est! Omnes informationes supradictae ad solam referentiam sunt, nec ut dux pro opere institutorum medicorum vel unitatum affinium adhibendae sunt. Alioquin, quaevis consequentiae ab hac societate effectae nihil ad hanc societatem pertinent.