Primary Device ID | 00858395006271 |
NIH Device Record Key | 434b3844-3065-40b2-99b3-ed3c4ad24370 |
Commercial Distribution Discontinuation | 2016-09-07 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Molar Treatment Instrument |
Version Model Number | FG-001-00001 |
Catalog Number | GW-MOL-TIXX |
Company DUNS | 828894373 |
Company Name | SONENDO, 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 | 8447663636 |
info@sonendo.com |
Storage Environment Temperature | Between 10 Degrees Celsius and 40 Degrees Celsius |
Storage Environment Temperature | Between 10 Degrees Celsius and 40 Degrees Celsius |
Storage Environment Temperature | Between 10 Degrees Celsius and 40 Degrees Celsius |
Storage Environment Temperature | Between 10 Degrees Celsius and 40 Degrees Celsius |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00858395006271 [Primary] |
ELC | Scaler, Ultrasonic |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-08-03 |
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