Primary Device ID | 10607567109541 |
NIH Device Record Key | accae1cf-95ca-4e98-b3a6-7e0aa4a51e30 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sensation 7FR. 34cc IAB with Accessories, US Only |
Version Model Number | 0684-00-0469-01U |
Catalog Number | 0684-00-0469-01U |
Company DUNS | 001660786 |
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 | true |
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 | true |
OTC Over-The-Counter | false |
Phone | 888-627-8383 |
customer.support@maquet.com | |
Phone | 888-627-8383 |
customer.support@maquet.com | |
Phone | 888-627-8383 |
customer.support@maquet.com | |
Phone | 888-627-8383 |
customer.support@maquet.com | |
Phone | 888-627-8383 |
customer.support@maquet.com | |
Phone | 888-627-8383 |
customer.support@maquet.com | |
Phone | 888-627-8383 |
customer.support@maquet.com | |
Phone | 888-627-8383 |
customer.support@maquet.com | |
Phone | 888-627-8383 |
customer.support@maquet.com | |
Phone | 888-627-8383 |
customer.support@maquet.com | |
Phone | 888-627-8383 |
customer.support@maquet.com | |
Phone | 888-627-8383 |
customer.support@maquet.com | |
Phone | 888-627-8383 |
customer.support@maquet.com | |
Phone | 888-627-8383 |
customer.support@maquet.com |
Catheter Gauge | 7 French |
Catheter Gauge | 7 French |
Catheter Gauge | 7 French |
Catheter Gauge | 7 French |
Catheter Gauge | 7 French |
Catheter Gauge | 7 French |
Catheter Gauge | 7 French |
Catheter Gauge | 7 French |
Catheter Gauge | 7 French |
Catheter Gauge | 7 French |
Catheter Gauge | 7 French |
Catheter Gauge | 7 French |
Catheter Gauge | 7 French |
Catheter Gauge | 7 French |
Device Issuing Agency | Device ID |
---|---|
GS1 | 10607567109541 [Primary] |
DSP | System, Balloon, Intra-Aortic And Control |
Steralize Prior To Use | true |
Device Is Sterile | true |
[10607567109541]
Ethylene Oxide
[10607567109541]
Ethylene Oxide
[10607567109541]
Ethylene Oxide
[10607567109541]
Ethylene Oxide
[10607567109541]
Ethylene Oxide
[10607567109541]
Ethylene Oxide
[10607567109541]
Ethylene Oxide
[10607567109541]
Ethylene Oxide
[10607567109541]
Ethylene Oxide
[10607567109541]
Ethylene Oxide
[10607567109541]
Ethylene Oxide
[10607567109541]
Ethylene Oxide
[10607567109541]
Ethylene Oxide
[10607567109541]
Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2021-12-06 |
Device Publish Date | 2016-09-15 |
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10607567113784 - CABLE,LOW LEVEL OUTPUT,GE | 2024-08-05 |
10607567113807 - CABLE,INTERFACE,1/4-1/4",30' | 2024-08-05 |
10607567113814 - CABLE, INTERFACE .25" PLUG TO .25" PLUG 30 | 2024-08-05 CABLE, INTERFACE 1/4" PLUG TO 1/4" PLUG 30 |
10607567113821 - CABLE, INTERFACE 1/4” PLUG TO 1/8” PLUG, | 2024-08-05 |