Primary Device ID | 00817602022640 |
NIH Device Record Key | 89d6773a-7454-4237-8e8e-6aa4ac67a101 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CCore |
Version Model Number | 16008 |
Catalog Number | 16008 |
Company DUNS | 096989103 |
Company Name | C-CORE MEDICAL, 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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00817602022633 [Primary] |
GS1 | 00817602022640 [Package] Contains: 00817602022633 Package: Case [18 Units] In Commercial Distribution |
KKX | Drape, Surgical |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-10-05 |
Device Publish Date | 2020-09-25 |
00817602022664 | Drape, Ortho, Beach Chair |
00817602022640 | Cover, Table Drape |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() CCORE 97836351 not registered Live/Pending |
IMPAQ ENTREPRENEUR, INC. 2023-03-13 |
![]() CCORE 86592342 4929010 Live/Registered |
Jatheon Technologies, Inc. 2015-04-09 |
![]() CCORE 86324427 not registered Dead/Abandoned |
Jatheon Technologies, Inc. 2014-06-30 |
![]() CCORE 74440664 1900822 Live/Registered |
RESPONSE DESIGN CORPORATION 1993-09-27 |