Primary Device ID | 00684995530010 |
NIH Device Record Key | d0fe648e-117c-40d4-ad4d-da415586127f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Silicone Tubing, Translucent |
Version Model Number | GS75160-03 |
Company DUNS | 080524654 |
Company Name | BENTEC MEDICAL OPCO, LLC |
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 | 00684995530010 [Primary] |
GBX | Catheter, Irrigation |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-10-30 |
Device Publish Date | 2023-10-20 |
00684995530201 | 28 Fr. x 100 cm |
00684995530195 | 26 Fr. x 100 cm |
00684995530188 | 24 Fr. x 100 cm |
00684995530171 | 22 Fr. x 100 cm |
00684995530164 | 20 Fr. x 100 cm |
00684995530157 | 19 Fr. x 100 cm |
00684995530140 | 18 Fr. x 100 cm |
00684995530133 | 16 Fr. x 100 cm |
00684995530126 | 15 Fr. x 100 cm |
00684995530119 | 14 Fr. x 100 cm |
00684995530102 | 12 Fr. x 100 cm |
00684995530089 | 10 Fr. x 100 cm |
00684995530072 | 9 Fr. x 100 cm |
00684995530065 | 8 Fr. x 100 cm |
00684995530058 | 7 Fr. x 100 cm |
00684995530041 | 6 Fr. x 100 cm |
00684995530034 | 5 Fr. x 100 cm |
00684995530027 | 4 Fr. x 100 cm |
00684995530010 | 3 Fr. x 100 cm |