Primary Device ID | 00884838107403 |
NIH Device Record Key | f0696e15-9a8e-49f6-9345-f72f491d373a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DA200ULTRA+LMB |
Version Model Number | 9890-000-87331 |
Catalog Number | 9890-000-87331 |
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 |