Primary Device ID | 08714729260325 |
NIH Device Record Key | 87e4e2e9-480e-496a-8ce4-dbf9a972a40f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Maverick® |
Version Model Number | H7492062012300 |
Company DUNS | 021717889 |
Company Name | BOSTON SCIENTIFIC CORPORATION |
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 | 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 | true |
OTC Over-The-Counter | false |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08714729260325 [Primary] |
LOX | Catheters, transluminal coronary angioplasty, percutaneous |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-10-07 |
Device Publish Date | 2016-09-24 |
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08714729260325 | PTCA Dilatation Catheter |
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08714729260301 | PTCA Dilatation Catheter |
08714729260295 | PTCA Dilatation Catheter |
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