Primary Device ID | 04048675224334 |
NIH Device Record Key | 1963db07-c91d-4f3b-af8b-8d4abeb638c9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | BlueSet Anesthesia WT (P/A) |
Version Model Number | MK04248 |
Company DUNS | 315578914 |
Company Name | Drägerwerk AG & Co. KGaA |
Device Count | 1 |
DM Exempt | true |
Pre-market Exempt | true |
MRI Safety Status | MR Unsafe |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Phone | +494518820 |
INFO@DRAEGER.COM |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04048675224334 [Primary] |
BTC | Bag, Reservoir |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-12-11 |
Device Publish Date | 2017-08-24 |
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