Primary Device ID | 00884838025738 |
NIH Device Record Key | 53cbd286-fbf1-4b63-ba33-c90f4d3f5d97 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Philips Respironics |
Version Model Number | V60 |
Catalog Number | U1053617 |
Company DUNS | 079550876 |
Company Name | Respironics California, 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 | false |
Serial Number | true |
Manufacturing Date | false |
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 |
Handling Environment Temperature | Between -20 Degrees Celsius and 60 Degrees Celsius |
Handling Environment Temperature | Between -20 Degrees Celsius and 60 Degrees Celsius |
Handling Environment Temperature | Between -20 Degrees Celsius and 60 Degrees Celsius |
Handling Environment Temperature | Between -20 Degrees Celsius and 60 Degrees Celsius |
Handling Environment Temperature | Between -20 Degrees Celsius and 60 Degrees Celsius |
Handling Environment Temperature | Between -20 Degrees Celsius and 60 Degrees Celsius |
Handling Environment Temperature | Between -20 Degrees Celsius and 60 Degrees Celsius |