Primary Device ID | 00606959050730 |
NIH Device Record Key | 22e1ba0f-cf88-4a32-a710-8f45f5b1dd89 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Care Orchestrator Software |
Version Model Number | 1.13 |
Catalog Number | 1126366 |
Company DUNS | 080728314 |
Company Name | Respironics, 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 | true |
OTC Over-The-Counter | false |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx | |
Phone | +1(999)999-9999 |
xx@xx.xx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00606959050730 [Primary] |
BZD | VENTILATOR, NON-CONTINUOUS (RESPIRATOR) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-11-08 |
Device Publish Date | 2018-04-16 |
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