Primary Device ID | 08714729479109 |
NIH Device Record Key | a60b0065-eb53-472a-a162-e0fbba749e6e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | EZ Bent Tip |
Version Model Number | H749501001500 |
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 | 08714729479109 [Primary] |
NFA | Temporary Coronary Saphenous Vein Bypass Graft for Embolic Protection |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-04-09 |
Device Publish Date | 2016-09-24 |
08714729035404 - NA | 2024-06-06 Arterial Entry Needle |
08714729035411 - NA | 2024-06-06 Arterial Entry Needle |
08714729841692 - Rhythmia™ Mapping System | 2024-06-06 ECG Cable - Trunk - US AAMI |
08714729841715 - Rhythmia™ Mapping System | 2024-06-06 ECG Cable - Limbs - US AAMI |
08714729841739 - Rhythmia™ Mapping System | 2024-06-06 ECG Cable - Chest - US AAMI |
08714729938507 - RHYTHMIA HDx™ | 2024-06-06 ECG IN Cable (Trunk) |
08714729938514 - RHYTHMIA HDx™ | 2024-06-06 ECG IN Cable (Trunk) |
08714729938521 - RHYTHMIA HDx™ | 2024-06-06 ECG IN Cable (Limb and Chest) |