Primary Device ID | 05707480041152 |
NIH Device Record Key | 8542f41e-0d4e-42db-874e-a92cdc4f85bf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SleepmateRIPmate Cable |
Version Model Number | 819150-000 |
Catalog Number | 819150-000 |
Company DUNS | 305682023 |
Company Name | Ambu A/S |
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 | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +14107686464 |
Purchase_orders@ambuUSA.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05707480041152 [Primary] |
GS1 | 05707480096893 [Direct Marking] |
BZQ | Monitor, breathing frequency |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2018-10-29 |
Device Publish Date | 2016-09-21 |
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