Primary Device ID | D040200121301 |
NIH Device Record Key | b4c7ee1c-2931-4bbd-952c-ffa90fad5bd1 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Pulse oximeter |
Version Model Number | 20012130 |
Company DUNS | 006385173 |
Company Name | WHIP-MIX 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 | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | true |
Serial Number | true |
Manufacturing Date | true |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |