Primary Device ID | 00192896121393 |
NIH Device Record Key | eabe700c-d6e0-4a3b-abe4-b4fa28e27a16 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Dental Elevator Combo Set |
Version Model Number | 1102-2000-SET |
Catalog Number | 1102-2000-SET |
Company DUNS | 040729840 |
Company Name | SONTEC INSTRUMENTS, INC. |
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 | false |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com | |
Phone | +1(800)821-7496 |
info@sontecinstruments.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00192896121393 [Primary] |
DZN | INSTRUMENTS, DENTAL HAND |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00192896121393]
Dry Heat Sterilization
[00192896121393]
Dry Heat Sterilization
[00192896121393]
Dry Heat Sterilization
[00192896121393]
Dry Heat Sterilization
[00192896121393]
Dry Heat Sterilization
[00192896121393]
Dry Heat Sterilization
[00192896121393]
Dry Heat Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-04-21 |
Device Publish Date | 2025-04-11 |
00192896121409 | Dental Elevator Combo Set With Tray |
00192896121393 | Dental Elevator Combo Set Without Tray |