Primary Device ID | 00884838075955 |
NIH Device Record Key | 504bc913-a1bb-44eb-a34f-0bd62f34b21e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SRO 0950 ROT 350 |
Version Model Number | 9874-007-01122 |
Catalog Number | 9874-007-01122 |
Company DUNS | 314101218 |
Company Name | Philips Medical Systems DMC GmbH |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | true |
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 | false |
OTC Over-The-Counter | false |