Primary Device ID | 07540198003115 |
NIH Device Record Key | 11f6e91c-df01-433d-9c57-94c73108db4f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | FlexTube |
Version Model Number | Connector |
Catalog Number | 8232-50 |
Company DUNS | 250896255 |
Company Name | Prime Pacific Health Innovations Corporation |
Device Count | 50 |
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 | 07540198003023 [Primary] |
GS1 | 07540198003115 [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 |