| Primary Device ID | 00192896024472 |
| NIH Device Record Key | 59b1c4c7-a051-44bf-aa69-a69f6fee1c47 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | UNIVERSAL PROBE |
| Version Model Number | 197-683 |
| Catalog Number | 197-683 |
| 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 | false |
| 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 | |
| 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 | |
| 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 |
| Length | 7 Inch |
| Length | 7 Inch |
| Length | 7 Inch |
| Length | 7 Inch |
| Length | 7 Inch |
| Length | 7 Inch |
| Length | 7 Inch |
| Length | 7 Inch |
| Length | 7 Inch |
| Length | 7 Inch |
| Length | 7 Inch |
| Length | 7 Inch |
| Length | 7 Inch |
| Length | 7 Inch |
| Length | 7 Inch |
| Length | 7 Inch |
| Length | 7 Inch |
| Length | 7 Inch |
| Length | 7 Inch |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00192896024472 [Primary] |
| FGM | Probe And Director, Gastro-Urology |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00192896024472]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896024472]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896024472]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896024472]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896024472]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896024472]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896024472]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896024472]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896024472]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896024472]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896024472]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896024472]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896024472]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896024472]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896024472]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896024472]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896024472]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896024472]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[00192896024472]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-02-19 |
| Device Publish Date | 2018-09-14 |
| 00192896076655 | UNIVERSAL PROBE WITH EYE SILVER |
| 00192896076648 | UNIVERSAL PROBE SILVER DOUBLE ENDED MALLEABLE |
| 00192896024489 | UNIVERSAL PROBE WITH EYE SILVER |
| 00192896024472 | UNIVERSAL PROBE WITH EYE SILVER |
| 00192896024465 | UNIVERSAL PROBE WITH EYE SILVER |
| 00192896024458 | UNIVERSAL PROBE DOUBLE ENDED MALLEABLE SILVER |
| 00192896024441 | UNIVERSAL PROBE DOUBLE ENDED STAINLESS STEEL |
| 00192896024434 | UNIVERSAL PROBE DOUBLE ENDED MALLEABLE SILVER |
| 00192896024427 | UNIVERSAL PROBE DOUBLE ENDED STAINLESS STEEL |
| 00192896024410 | UNIVERSAL PROBE DOUBLE ENDED STAINLESS STEEL |
| 00192896024403 | UNIVERSAL PROBE DOUBLE ENDED STAINLESS STEEL |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() UNIVERSAL PROBE 86336744 not registered Dead/Abandoned |
Sohwa & Sophia Technologies Inc. 2014-07-14 |