Primary Device ID | 05030267159796 |
NIH Device Record Key | cda7ff9a-43a5-4f2c-9940-0809697aafe6 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SENTRI, PAEDIATRIC, NASAL CANNULA WITH CURVED PRONGS, CO2 MONITORING LINE |
Version Model Number | 1144015 |
Company DUNS | 785952607 |
Company Name | Intersurgical Incorporated |
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 | false |
Device Combination Product | true |
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 |
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