Primary Device ID | 00606959049925 |
NIH Device Record Key | 2d349a55-3636-445e-9533-6d906d60ea34 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | DreamMapper Android China Instance v 2.11 |
Version Model Number | 2.11 |
Catalog Number | 1136947 |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00606959049925 [Primary] |
BZD | VENTILATOR, NON-CONTINUOUS (RESPIRATOR) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2019-04-29 |
Device Publish Date | 2019-04-19 |
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