Primary Device ID | 08714729877899 |
NIH Device Record Key | 0bcb306f-a902-4f0f-80b6-c1f0a0bc7bd4 |
Commercial Distribution Discontinuation | 2020-04-25 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Radia™ |
Version Model Number | M004320014G0 |
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 Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 08714729877899 [Primary] |
DRF | CATHETER, ELECTRODE RECORDING, OR PROBE, ELECTRODE RECORDING |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2025-01-08 |
Device Publish Date | 2016-09-24 |
08714729880004 | Bidirectional Steerable Diagnostic Catheter |
08714729879992 | Bidirectional Steerable Diagnostic Catheter |
08714729877950 | Bidirectional Steerable Diagnostic Catheter |
08714729877936 | Bidirectional Steerable Diagnostic Catheter |
08714729877929 | Bidirectional Steerable Diagnostic Catheter |
08714729877912 | Bidirectional Steerable Diagnostic Catheter |
08714729877905 | Bidirectional Steerable Diagnostic Catheter |
08714729877899 | Bidirectional Steerable Diagnostic Catheter |
08714729877882 | Bidirectional Steerable Diagnostic Catheter |
08714729877875 | Bidirectional Steerable Diagnostic Catheter |
08714729877868 | Bidirectional Steerable Diagnostic Catheter |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
RADIA 98718714 not registered Live/Pending |
RADIA, INC. 2024-08-27 |
RADIA 98491882 not registered Live/Pending |
RADIA INC., P.S. 2024-04-09 |
RADIA 97906521 not registered Live/Pending |
Steelcase Inc. 2023-04-25 |
RADIA 97797665 not registered Live/Pending |
Al. Neyer, LLC 2023-02-16 |
RADIA 97501277 not registered Live/Pending |
1Vibe Inc. 2022-07-13 |
RADIA 97251701 not registered Live/Pending |
OnProcess Technology, Inc. 2022-02-03 |
RADIA 90631520 not registered Live/Pending |
Radia, Inc. 2021-04-08 |
RADIA 88940393 not registered Live/Pending |
Radia, Inc. 2020-05-29 |
RADIA 88428995 not registered Live/Pending |
Neuvana, LLC 2019-05-14 |
RADIA 88211330 not registered Live/Pending |
CAMBRIGE OVERSEAS DEVELOPMENT INC. 2018-11-29 |
RADIA 87687330 not registered Live/Pending |
Radia, Inc. 2017-11-16 |
RADIA 86326848 5008568 Live/Registered |
Red Devil Equipment Company 2014-07-02 |