Primary Device ID | 10859911004792 |
NIH Device Record Key | c855d58a-9986-4466-b347-17a2f8ece7d5 |
Commercial Distribution Discontinuation | 2025-09-08 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Tabletop Waterpik Adapter Wands |
Version Model Number | 27210 |
Catalog Number | 27210 |
Company DUNS | 117844489 |
Company Name | Bionix, LLC |
Device Count | 3 |
DM Exempt | true |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | false |
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)551-7096 |
Bionix@bionix.com | |
Phone | +1(800)551-7096 |
Bionix@bionix.com | |
Phone | +1(800)551-7096 |
Bionix@bionix.com | |
Phone | +1(800)551-7096 |
Bionix@bionix.com | |
Phone | +1(800)551-7096 |
Bionix@bionix.com | |
Phone | +1(800)551-7096 |
Bionix@bionix.com | |
Phone | +1(800)551-7096 |
Bionix@bionix.com | |
Phone | +1(800)551-7096 |
Bionix@bionix.com | |
Phone | +1(800)551-7096 |
Bionix@bionix.com | |
Phone | +1(800)551-7096 |
Bionix@bionix.com | |
Phone | +1(800)551-7096 |
Bionix@bionix.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00859911004795 [Primary] |
GS1 | 10859911004792 [Unit of Use] |
LRD | APPLICATOR, ENT DRUG |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2025-09-09 |
Device Publish Date | 2024-07-11 |
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