Nellcor Compatible Disposable SpO2 Sensor Adult/Neonatal Non-Woven
Parameter of A1418-SN03M Disposable SpO2 Sensor
Product Name | Disposable SpO2 Sensor |
| Compatible Brand | Nellcor (NON-Oximax) N550, N595 |
Application | Medical Patient Monitoring |
Parameter | SpO2 |
Cable Color | White |
Cable Material | Medical Grade PVC |
Total Cable Length | 50-90cm |
Sensor Wavelength and Output Power | Red: 660 nm at 1-5 mW nominal |
Sensor Wavelength and Output Power | IR: 905 nm at 1-5 mW nominal |
Patiend-end Size | Neonatal |
Macine-end Connector | DB9(9pin), OxiMax |
APK Part No. | Product Description |
A1418-SA01M | Nellcor Compatible Adult Disposable SpO2 Sensor DB9 9pin 3M Foam or Microfoam |
A1418-SP01M | Nellcor Compatible Pediatric Disposable SpO2 Sensor DB9 9pin 3M Foam or Microfoam |
A1418-SI01M | Nellcor Compatible Infant Disposable SpO2 Sensor DB9 9pin 3M Foam or Microfoam |
A1418-SN01M | Nellcor Compatible Neonatal Disposable SpO2 Sensor DB9 9pin 3M Foam or Microfoam |
A1418-SA02M | Nellcor Compatible Adult Disposable SpO2 Sensor DB9 9pin Spon |
| A1418-SP02M | Nellcor Compatible Pediatric Disposable SpO2 Sensor DB9 9pin Sponge |
A1418-SI02M | Nellcor Compatible Infant Disposable SpO2 Sensor DB9 9pin Sponge |
A1418-SN02M | Nellcor Compatible Neonatal Disposable SpO2 Sensor DB9 9pin Sponge |
A1418-SA03M | Nellcor Compatible Adult Disposable SpO2 Sensor DB9 9pin Non woven Fabric |
A1418-SP03M | Nellcor Compatible Pediatric Disposable SpO2 Sensor DB9 9pin Non woven Fabric |
A1418-SI03M | Nellcor Compatible Infant Disposable SpO2 Sensor DB9 9pin Non woven Fabric |
A1418-SN03M | Nellcor Compatible Neonatal Disposable SpO2 Sensor DB9 9pin Non woven Fabric |
Production Process | Injection Molding, Not Assembly |
Quality | APK meets a worldwide range of standards that have been set by regulatory authorities and standardizations committees. Please contact us for more details. We are very glad to send you our latest price list and share updated medical industry information. Factory audit, product test report and certifications will be sent at the same time. |
Factory Audit | ISO13485, Medical Device Regulation(EU)2017/745, Brazil ANVISA, USA Welch Allyn, MDSAP |
Product Test Report | 1， IEC 60601-1-2 Test Report, IEC 60601-1 Test Report、ISO 80601-2-61 Test Report。 2， Clinical Trial Report。 3， Biocompatibility Test Report, Cytotoxicity Test, Skin Sensitization Test, Skin Irritancy Test。 |
Certification | Conformite Europeenne, Comply with Food and Drug Administration Regulations |
