Primary Device ID | 20610075104448 |
NIH Device Record Key | fa91141b-9009-462d-85cb-b85b3b0c0788 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | InstantCath |
Version Model Number | 9675 |
Catalog Number | 9675 |
Company DUNS | 005527098 |
Company Name | HOLLISTER INCORPORATED |
Device Count | 30 |
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 | true |
OTC Over-The-Counter | false |
Phone | +1(800)323-4060 |
CS@Hollister.com | |
Phone | +1(800)323-4060 |
CS@Hollister.com | |
Phone | +1(800)323-4060 |
CS@Hollister.com | |
Phone | +1(800)323-4060 |
CS@Hollister.com | |
Phone | +1(800)323-4060 |
CS@Hollister.com | |
Phone | +1(800)323-4060 |
CS@Hollister.com | |
Phone | +1(800)323-4060 |
CS@Hollister.com | |
Phone | +1(800)323-4060 |
CS@Hollister.com | |
Phone | +1(800)323-4060 |
CS@Hollister.com |
Catheter Length | 20 Centimeter |
Catheter Gauge | 12 French |
Catheter Length | 20 Centimeter |
Catheter Gauge | 12 French |
Catheter Length | 20 Centimeter |
Catheter Gauge | 12 French |
Catheter Length | 20 Centimeter |
Catheter Gauge | 12 French |
Catheter Length | 20 Centimeter |
Catheter Gauge | 12 French |
Catheter Length | 20 Centimeter |
Catheter Gauge | 12 French |
Catheter Length | 20 Centimeter |
Catheter Gauge | 12 French |
Catheter Length | 20 Centimeter |
Catheter Gauge | 12 French |
Catheter Length | 20 Centimeter |
Catheter Gauge | 12 French |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00610075067237 [Unit of Use] |
GS1 | 00610075104444 [Primary] |
GS1 | 20610075104448 [Package] Contains: 00610075104444 Package: Case [18 Units] In Commercial Distribution |
GBM | CATHETER, URETHRAL |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-07-17 |
Device Publish Date | 2024-07-09 |
20610075104479 | Pre-lubricated Urethral Intermittent Catheter |
20610075104455 | Pre-lubricated Urethral Intermittent Catheter |
20610075104448 | Pre-lubricated Urethral Intermittent Catheter |
20610075104431 | Pre-lubricated Urethral Intermittent Catheter |
25390166097587 | Pre-lubricated Urethral Intermittent Catheter |
20610075104417 | Pre-lubricated Urethral Intermittent Catheter |
20610075104400 | Pre-lubricated Urethral Intermittent Catheter |
20610075104394 | Pre-lubricated Urethral Intermittent Catheter |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
![]() INSTANTCATH 77179889 not registered Dead/Abandoned |
MEDICAL TECHNOLOGIES OF GEORGIA, INC. 2007-05-14 |
![]() INSTANTCATH 75869413 2396034 Dead/Cancelled |
MEDICAL TECHNOLOGIES OF GEORGIA, INC. 1999-12-08 |
![]() INSTANTCATH 75858600 2395957 Dead/Cancelled |
MEDICAL TECHNOLOGIES OF GEORGIA, INC. 1999-11-26 |