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 |