Primary Device ID | 00850041415161 |
NIH Device Record Key | 68b044fa-7058-4d82-b15b-3c5668470331 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | ClearTract |
Version Model Number | 211810SPT |
Company DUNS | 080312381 |
Company Name | PATHWAY, LLC |
Device Count | 1 |
DM Exempt | false |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00850041415161 [Primary] |
EZL | Catheter, Retention Type, Balloon |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2024-05-29 |
Device Publish Date | 2024-05-21 |
00850041415161 | 2-Way 100% Silicone, 18Fr X 10ml, ClearTract SPT Catheter |
00850041415154 | 2-Way 100% Silicone, 16Fr X 10ml, ClearTract SPT Catheter |
00850041415147 | 2-Way 100% Silicone, 16Fr X 5ml, ClearTract SPT Catheter |
00850041415130 | 2-Way 100% Silicone, 14Fr X 10ml, ClearTract SPT Catheter |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
CLEARTRACT 88806495 not registered Live/Pending |
Hydrophilix, Inc. 2020-02-21 |
CLEARTRACT 85378458 4111610 Dead/Cancelled |
Discover Nutrition, Inc. 2011-07-22 |
CLEARTRACT 78382198 not registered Dead/Abandoned |
Versprille, Evan K. 2004-03-11 |