Primary Device ID | 00643169359888 |
NIH Device Record Key | f2ae30d8-5665-4b1f-bb33-a47f5701befb |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Micra™ Introducer |
Version Model Number | MI2355A |
Company DUNS | 006261481 |
Company Name | MEDTRONIC, 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 | false |
Expiration Date | false |
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(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.com | |
Phone | +1(800)633-8766 |
Corporate.UDI@medtronic.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 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 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 | 00643169359888 [Primary] |
DYB | INTRODUCER, CATHETER |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-06-07 |
Device Publish Date | 2016-08-07 |
00763000976408 - NA | 2024-09-24 CUSTOM PACK 6W69R14 ADULT PACK |
00763000976415 - NA | 2024-09-24 CUSTOM PACK BB10V39R5 PEDI Q |
00763000976422 - NA | 2024-09-24 CUSTOM PACK BB11D79R4 UCSFMB SUPPOR |
00763000976439 - NA | 2024-09-24 CUSTOM PACK BB10G17R10 E INFANT |
00763000976460 - NA | 2024-09-24 CUSTOM PACK BB7C02R27 PMP/TBL |
00763000974749 - NA | 2024-09-23 CUSTOM PACK BB10Y59R11 FUSION |
00763000974978 - NA | 2024-09-23 CUSTOM PACK BB11X52R6 PUMP TABLE V2 |
20763000975177 - NA | 2024-09-23 CUSTOM PACK BB12J41R 5PK VEN CAN STUB L |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
MICRA 86794383 not registered Live/Pending |
Nissan Jidosha Kabushiki Kaisha 2015-10-21 |
MICRA 85715767 4568896 Live/Registered |
Medtronic, Inc. 2012-08-29 |
MICRA 85646130 4584996 Live/Registered |
Medtronic, Inc. 2012-06-07 |
MICRA 85373179 not registered Dead/Abandoned |
Shiela Nail Products, Inc. 2011-07-16 |
MICRA 85373179 not registered Dead/Abandoned |
J-mar International 2011-07-16 |
MICRA 79048392 3492995 Dead/Cancelled |
CONTROLLI S.P.A. 2007-12-20 |
MICRA 78363412 not registered Dead/Abandoned |
Microeconomic Consulting & Research Associates, Inc. 2004-02-05 |
MICRA 77577332 3688412 Dead/Cancelled |
Nissan Jidosha Kabushiki Kaisha 2008-09-24 |
MICRA 76438044 2715711 Dead/Cancelled |
KIDDE PRODUCTS LIMITED 2002-08-05 |
MICRA 76303416 2741079 Dead/Cancelled |
Montegrappa 1912 S.p.A. 2001-08-22 |
MICRA 75871337 2622792 Dead/Cancelled |
NISSAN JIDOSHA KABUSHIKI KAISHA 1999-12-14 |
MICRA 75639758 not registered Dead/Abandoned |
NISSAN JIDOSHA KABUSHIKI KAISHA 1999-02-11 |