Primary Device ID | 00195949116209 |
NIH Device Record Key | e891b120-d4a1-414e-bf22-fd88e2c95644 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sleep Apnea Notification Feature (SANF) |
Version Model Number | Feature version 1.X |
Company DUNS | 060704780 |
Company Name | APPLE INC. |
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 | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | true |