Primary Device ID | 00842429118092 |
NIH Device Record Key | 4819634b-273b-4d65-b0b6-f53b5963ae8f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Access |
Version Model Number | ISC5115ST-RA |
Catalog Number | ISC5115ST |
Company DUNS | 003263105 |
Company Name | MICROVENTION INC. |
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 | 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 | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com | |
Phone | +1(714) 247-8000 |
customerservice@microvention.com |
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 | 00842429118092 [Primary] |
DQY | Catheter, percutaneous |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-10-28 |
Device Publish Date | 2024-10-18 |
00842429108444 - Sofia | 2024-10-28 Sofia 6F-115cm STR |
00842429108451 - Sofia | 2024-10-28 Sofia 6F-125cm STR |
00842429108468 - Sofia | 2024-10-28 Sofia 6F-131cm STR |
00842429108475 - Sofia | 2024-10-28 Sofia 6F-125cm STR |
00842429118092 - Access | 2024-10-28Sofia EX 5F - 115cm STR |
00842429118092 - Access | 2024-10-28 Sofia EX 5F - 115cm STR |
00842429119396 - Wedge | 2024-10-28 Wedge XL |
00842429108482 - Sofia | 2024-08-14 Sofia 6F-131cm STR |
00842429117705 - SOFIA 88 | 2023-06-23 SOFIA 88 - 115cm |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ACCESS 98849021 not registered Live/Pending |
Access Members, Inc. 2024-11-12 |
ACCESS 98604507 not registered Live/Pending |
Better Earth LLC 2024-06-17 |
ACCESS 98301775 not registered Live/Pending |
Access Group, Inc. 2023-12-06 |
ACCESS 98289355 not registered Live/Pending |
Penumbra, Inc. 2023-11-28 |
ACCESS 98182378 not registered Live/Pending |
Troy and Sabina Benavides 2023-09-15 |
ACCESS 98017184 not registered Live/Pending |
Sony Interactive Entertainment Inc. 2023-05-28 |
ACCESS 97936930 not registered Live/Pending |
Winnebago Industries, Inc. 2023-05-15 |
ACCESS 97792738 not registered Live/Pending |
Piv Train Inc 2023-02-13 |
ACCESS 97756255 not registered Live/Pending |
Coppel S.A. de C.V. 2023-01-16 |
ACCESS 97202119 not registered Live/Pending |
Access Alternative Investments, Inc. 2022-01-04 |
ACCESS 97180047 not registered Live/Pending |
Wicket, LLC 2021-12-20 |
ACCESS 90827919 not registered Live/Pending |
Access Eforms, LP 2021-07-14 |