Primary Device ID | 10843997001066 |
NIH Device Record Key | d5cbbe07-db56-4d55-8e71-4bd56c855593 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MasimoSET® LNOP® Sensors application training packet |
Version Model Number | 1282 |
Company DUNS | 780421038 |
Company Name | MASIMO CORPORATION |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
00843997017688 - Nomoline | 2024-03-27 NomoLine LH Bypass Tubing, 3m |
00843997005364 - Masimo W1 | 2024-03-11 Masimo W1, Tele-Health, Global |
00843997017480 - Masimo W1 | 2024-03-11 Masimo W1, Global, France |
00843997017497 - Masimo W1 | 2024-03-11 Masimo W1, Global, German |
00843997017503 - Masimo W1 | 2024-03-11 Masimo W1, Global, Switzerland |
00843997017510 - Masimo W1 | 2024-03-11 Masimo W1, Global, Italy |
00843997017527 - Masimo W1 | 2024-03-11 Masimo W1, Global, Sweden |
00843997017534 - Masimo W1 | 2024-03-11 Masimo W1, Global, Netherlands |