Primary Device ID | 20677964060377 |
NIH Device Record Key | 51ad27c2-e85b-4c9e-80f6-429394172255 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Backflow Valve Connector |
Version Model Number | 100126P |
Company DUNS | 068199363 |
Company Name | MEDIVATORS INC. |
Device Count | 1 |
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 | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)444-4729 |
custserv@MEDIVATORS.com | |
Phone | +1(800)444-4729 |
custserv@MEDIVATORS.com | |
Phone | +1(800)444-4729 |
custserv@MEDIVATORS.com | |
Phone | +1(800)444-4729 |
custserv@MEDIVATORS.com | |
Phone | +1(800)444-4729 |
custserv@MEDIVATORS.com | |
Phone | +1(800)444-4729 |
custserv@MEDIVATORS.com | |
Phone | +1(800)444-4729 |
custserv@MEDIVATORS.com | |
Phone | +1(800)444-4729 |
custserv@MEDIVATORS.com | |
Phone | +1(800)444-4729 |
custserv@MEDIVATORS.com | |
Phone | +1(800)444-4729 |
custserv@MEDIVATORS.com | |
Phone | +1(800)444-4729 |
custserv@MEDIVATORS.com | |
Phone | +1(800)444-4729 |
custserv@MEDIVATORS.com | |
Phone | +1(800)444-4729 |
custserv@MEDIVATORS.com | |
Phone | +1(800)444-4729 |
custserv@MEDIVATORS.com | |
Phone | +1(800)444-4729 |
custserv@MEDIVATORS.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00677964060373 [Primary] |
GS1 | 10677964060370 [Package] Contains: 00677964060373 Package: Carton [10 Units] In Commercial Distribution |
GS1 | 20677964060377 [Package] Contains: 00677964060373 Package: Case [50 Units] In Commercial Distribution |
OCX | Endoscopic Irrigation/Suction System |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2019-04-23 |
Device Publish Date | 2018-08-15 |
50677964151731 - Endo Carry-on Procedure Kit | 2025-10-06 Endo Carry-on Procedure Kit contains Intercept Bedside Kit, Drawstring Pad, Gauze, and Biohazard Sticker. |
50677964151748 - Endo Carry-on Procedure Kit | 2025-10-06 Endo Carry-on Procedure Kit contains Basin, Sponge, Drawstring Pad, Lubricant, Gauze, Channel Cleaning Brush, Suction Tubing, Go |
50677964151755 - Endo Carry-on Procedure Kit | 2025-10-06 Endo Carry-on Procedure Kit contains Intercept Bedside Kit, Defendo Olympus 5-piece Kit, Endo Carry-On Transport Pad, Lubricant, |
50677964151762 - Endo Carry-on Procedure Kit | 2025-10-06 Endo Carry-on Procedure Kit contains Intercept Bedside Kit, Defendo Olympus 4-piece Kit, Drawstring Pad, Lubricant, Gauze, Duosw |
50677964151779 - Endo Carry-on Procedure Kit | 2025-10-06 Endo Carry-on Procedure Kit contains Intercept Bedside Kit, STERIS Fuji 700 4-piece Kit, Defendo Fuji 700 Cleaning Adapter, Clea |
50677964151786 - Endo Carry-on Procedure Kit | 2025-10-06 Endo Carry-on Procedure Kit contains Intercept Bedside Kit, Defendo Fuji 700 5-piece Kit, Extra Absorbant Pad, Suction Tubing, a |
50677964151793 - Endo Carry-on Procedure Kit | 2025-10-06 Endo Carry-on Procedure Kit contains Intercept Bedside Kit, Extra Absorbant Pad, Gauze, Suction Tubing, Biohazard Sticker, and M |
50677964151809 - Endo Carry-on Procedure Kit | 2025-10-06 Endo Carry-on Procedure Kit contains Intercept Bedside Kit, Defendo Olympus 5-piece Kit, Endo Carry-On Transport Pad, Lubricant, |