Primary Device ID | 04048675290735 |
NIH Device Record Key | 62139d9f-74c3-48a0-8877-bec8a53c9a85 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Pressure reducer O2,PININDEX,Primus |
Version Model Number | 8603466 |
Company DUNS | 315578914 |
Company Name | Drägerwerk AG & Co. KGaA |
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 | true |
Manufacturing Date | true |
Expiration Date | true |
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 | 04048675290735 [Primary] |
CAN | Regulator, Pressure, Gas Cylinder |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-07-07 |
Device Publish Date | 2022-06-29 |
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