Primary Device ID | 04048675715498 |
NIH Device Record Key | 5409c291-59f3-4dac-a8f1-463e67d7aef9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Anesth Set ID Coax WT 210 (BagCone22) |
Version Model Number | MP16045 |
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 | true |
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 |