Primary Device ID | 04049098007924 |
NIH Device Record Key | c7f49983-7997-4b10-9269-5dbe17f650ce |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SHP UNT R50 RECORDER UNIVERSA |
Version Model Number | 5952630 |
Company DUNS | 788289952 |
Company Name | DRAEGER MEDICAL SYSTEMS, 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 | false |
Serial Number | true |
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 |
Phone | +18004372437 |
info@draeger.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04049098007924 [Primary] |
DSF | Recorder, Paper Chart |
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 | 2015-10-24 |
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