Primary Device ID | 04049098007993 |
NIH Device Record Key | 04a1f2fd-11ca-46e9-a298-aaa68b9ad2ad |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | MultiMed 5 pod, 1.5 m |
Version Model Number | 5950196 |
Company DUNS | 788289952 |
Company Name | DRAEGER MEDICAL SYSTEMS, 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 | false |
Serial Number | false |
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 | 04049098007993 [Primary] |
DRW | Adaptor, Lead Switching, Electrocardiograph |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-11-02 |
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