Primary Device ID | 00851831007009 |
NIH Device Record Key | d5d1aa27-40bf-4488-a0d3-8a1df2a35f62 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Picis Perioperative and Critical Care |
Version Model Number | 8.6 |
Company DUNS | 105505866 |
Company Name | PICIS CLINICAL SOLUTIONS, INC. |
Device Count | 1 |
DM Exempt | false |
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 | true |
Serial Number | false |
Manufacturing Date | true |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00851831007009 [Primary] |
NSX | Software, Transmission And Storage, Patient Data |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2017-04-14 |
00851831007009 | An EMR system used in high acuity areas of the hospital (OR, ICU, Preop, PACU). A patient record |
00851831007054 | An EMR system used in high acuity areas of the hospital (OR, ICU, Preop, PACU). A patient record |
00851831007078 | Picis Perioperative and Critical Care: An EMR system used in high acuity areas of the hospital ( |