| Primary Device ID | 07540198003016 |
| NIH Device Record Key | 16f24e56-dfdd-4df5-9647-9aa893fc5e47 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | FlexTube |
| Version Model Number | Connector |
| Catalog Number | 8232-25 |
| Company DUNS | 250896255 |
| Company Name | Prime Pacific Health Innovations Corporation |
| Device Count | 25 |
| 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 | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 07540198003016 [Primary] |
| GS1 | 07540198003108 [Unit of Use] |
| GCD | Connector, Catheter |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-11-06 |
| Device Publish Date | 2023-10-27 |
| 07540198003115 | The FlexTube is a connector intended to be used with the AquaWing Treatment Table. It fits the f |
| 07540198003016 | The FlexTube is a connector intended to be used with the AquaWing Treatment Table. It fits the f |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() FLEXTUBE 76369519 2806216 Dead/Cancelled |
Johnson Matthey, Inc. 2002-02-07 |
![]() FLEXTUBE 76315057 not registered Dead/Abandoned |
ENGELHARD CORPORATION 2001-09-20 |
![]() FLEXTUBE 75673108 2359821 Dead/Cancelled |
ALCATEL 1999-04-02 |
![]() FLEXTUBE 74306221 not registered Dead/Abandoned |
JAMES RIVER PAPER COMPANY, INC. 1992-08-21 |
![]() FLEXTUBE 73375651 1266846 Dead/Cancelled |
Flextube, Inc. 1982-07-20 |