Primary Device ID | 00858395006059 |
NIH Device Record Key | b854c9af-6142-4ee8-8f49-78a2dece8571 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Sealing Cap (Size 7) |
Version Model Number | FG-001-00007 |
Catalog Number | GW-MOL-SP07 |
Company DUNS | 828894373 |
Company Name | SONENDO, INC. |
Device Count | 20 |
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 |
Handling Environment Atmospheric Pressure | Between 69.7 KiloPascal and 106 KiloPascal |
Handling Environment Atmospheric Pressure | Between 69.7 KiloPascal and 106 KiloPascal |
Handling Environment Atmospheric Pressure | Between 69.7 KiloPascal and 106 KiloPascal |
Handling Environment Atmospheric Pressure | Between 69.7 KiloPascal and 106 KiloPascal |
Handling Environment Atmospheric Pressure | Between 69.7 KiloPascal and 106 KiloPascal |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00858395006059 [Primary] |
GS1 | 00858395006127 [Unit of Use] |
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 | 2016-09-23 |
00858395006394 | Sealing Caps attach to the Molar Procedure Instrument in order to properly setup the Procedure I |
00858395006059 | Sealing Caps attach to the Molar Procedure Instrument in order to properly setup the Procedure I |