| Primary Device ID | 00860009369405 |
| NIH Device Record Key | b525518f-7127-4d8e-ad07-d4b58cb62919 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Cathaid |
| Version Model Number | CA55 |
| Company DUNS | 080652513 |
| Company Name | Cathaid Incorporated |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00860009369405 [Primary] |
| GS1 | 00860009369412 [Package] Package: [12 Units] In Commercial Distribution |
| GS1 | 00860009369429 [Package] Package: [48 Units] In Commercial Distribution |
| KMK | Device, Intravascular Catheter Securement |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-07-18 |
| Device Publish Date | 2023-07-10 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() CATHAID 87493031 not registered Live/Pending |
Cathaid Inc. 2017-06-16 |
![]() CATHAID 76701961 not registered Dead/Abandoned |
PSI MEDICAL CATHETER CARE, LLC 2010-03-08 |