Primary Device ID | 00884450451724 |
NIH Device Record Key | c7f9054a-61ac-4927-aecd-9adde162d0fd |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HeartSpan® |
Version Model Number | 00884450451724 |
Catalog Number | FND-025-02/A |
Company DUNS | 184763290 |
Company Name | Merit Medical Systems, Inc. |
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 | false |
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 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00884450451724 [Primary] |
DRC | Trocar |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-11-09 |
Device Publish Date | 2020-10-30 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
HEARTSPAN 87043746 5064437 Live/Registered |
Merit Medical Systems, Inc. 2016-05-19 |
HEARTSPAN 77169337 3680277 Dead/Cancelled |
Thomas Medical Products, Inc. 2007-04-30 |