Primary Device ID | 10607567111995 |
NIH Device Record Key | 7e1d0c70-c05c-4c9c-9931-832f3dd06f39 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | POWER SUPPLY, REMOVABLE |
Version Model Number | 0014-00-0085 |
Catalog Number | 0014-00-0085 |
Company DUNS | 040874329 |
Company Name | Datascope Corp. |
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 | true |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10607567111995 [Primary] |
DSP | System, Balloon, Intra-Aortic And Control |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2020-02-06 |
Device Publish Date | 2016-09-19 |