| Primary Device ID | 10858015005490 |
| NIH Device Record Key | 90e26d22-733d-48b4-9ad5-bc8408fddd23 |
| Commercial Distribution Discontinuation | 2017-12-07 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | ImarC™ |
| Version Model Number | 040201 |
| Catalog Number | 040201 |
| Company DUNS | 883094039 |
| Company Name | Carbon Medical Technologies, Inc. |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | false |
| MRI Safety Status | MR Safe |
| 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 |
| Phone | 8882070262 |
| info@carbonmed.com | |
| Phone | 8882070262 |
| info@carbonmed.com | |
| Phone | 8882070262 |
| info@carbonmed.com | |
| Phone | 8882070262 |
| info@carbonmed.com | |
| Phone | 8882070262 |
| info@carbonmed.com | |
| Phone | 8882070262 |
| info@carbonmed.com | |
| Phone | 8882070262 |
| info@carbonmed.com | |
| Phone | 8882070262 |
| info@carbonmed.com | |
| Phone | 8882070262 |
| info@carbonmed.com | |
| Phone | 8882070262 |
| info@carbonmed.com | |
| Phone | 8882070262 |
| info@carbonmed.com | |
| Phone | 8882070262 |
| info@carbonmed.com | |
| Phone | 8882070262 |
| info@carbonmed.com | |
| Phone | 8882070262 |
| info@carbonmed.com | |
| Phone | 8882070262 |
| info@carbonmed.com | |
| Phone | 8882070262 |
| info@carbonmed.com | |
| Phone | 8882070262 |
| info@carbonmed.com | |
| Phone | 8882070262 |
| info@carbonmed.com | |
| Phone | 8882070262 |
| info@carbonmed.com | |
| Phone | 8882070262 |
| info@carbonmed.com | |
| Phone | 8882070262 |
| info@carbonmed.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Length | 4 Millimeter |
| Outer Diameter | 2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 4 Millimeter |
| Outer Diameter | 2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 4 Millimeter |
| Outer Diameter | 2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 4 Millimeter |
| Outer Diameter | 2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 4 Millimeter |
| Outer Diameter | 2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 4 Millimeter |
| Outer Diameter | 2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 4 Millimeter |
| Outer Diameter | 2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 4 Millimeter |
| Outer Diameter | 2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 4 Millimeter |
| Outer Diameter | 2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 4 Millimeter |
| Outer Diameter | 2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 4 Millimeter |
| Outer Diameter | 2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 4 Millimeter |
| Outer Diameter | 2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 4 Millimeter |
| Outer Diameter | 2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 4 Millimeter |
| Outer Diameter | 2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 4 Millimeter |
| Outer Diameter | 2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 4 Millimeter |
| Outer Diameter | 2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 4 Millimeter |
| Outer Diameter | 2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 4 Millimeter |
| Outer Diameter | 2 Millimeter |
| Device Size Text, specify | 0 |
| Length | 4 Millimeter |
| Outer Diameter | 2 Millimeter |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00858015005493 [Primary] |
| GS1 | 10858015005490 [Package] Contains: 00858015005493 Package: Carton [10 Units] Discontinued: 2017-12-07 Not in Commercial Distribution |
| NEU | Marker, Radiographic, Implantable |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2015-10-14 |
| 10858015005490 | Tissue Marker System - Stereotactic Delivery |
| 10858015005483 | Tissue Marker System - Core Delivery |
| 10858015005476 | Tissue Marker System - Core Delivery |
| 10858015005469 | Tissue Marker System - Core Delivery |
| 10858015005452 | Tissue Marker System - Stereotactic Delivery |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() IMARC 98710542 not registered Live/Pending |
Ingram Library Services LLC 2024-08-21 |
![]() IMARC 86773053 5076460 Live/Registered |
iMarc LLC 2015-09-30 |
![]() IMARC 85082379 4018179 Live/Registered |
Investors Mortgage Asset Recovery Company, LLC 2010-07-12 |
![]() IMARC 85082370 4021499 Live/Registered |
Investors Mortgage Asset Recovery Company, LLC 2010-07-12 |
![]() IMARC 79295819 not registered Live/Pending |
IMARC S.P.A. 2020-05-18 |
![]() IMARC 79046860 3547069 Live/Registered |
IMARC S.P.A. 2007-06-28 |
![]() IMARC 78825117 3295500 Live/Registered |
SANARUS TECHNOLOGIES, INC. 2006-02-28 |
![]() IMARC 78212759 2900705 Dead/Cancelled |
VERSO TECHNOLOGIES, INC. 2003-02-10 |
![]() IMARC 77322900 3507546 Dead/Cancelled |
Karen Clark & Company 2007-11-06 |
![]() IMARC 74725530 2072579 Dead/Cancelled |
IMARC, L.L.C. 1995-09-05 |