| Primary Device ID | 00192896093430 |
| NIH Device Record Key | 67ed36fb-0e90-4c8e-bdff-41d24177e2d2 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | TUBE SHAFT |
| Version Model Number | 2901-109L |
| Catalog Number | 2901-109L |
| Company DUNS | 040729840 |
| Company Name | SONTEC INSTRUMENTS, 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 | false |
| Lot Batch | false |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | true |
| 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 |
| Device Size Text, specify | 0 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00192896093430 [Primary] |
| GEI | Electrosurgical, cutting & coagulation & accessories |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00192896093430]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-04-26 |
| Device Publish Date | 2019-03-07 |
| 00192896092341 | TUBE SHAFT WITH LUER LOCK INSULATED CYLINDRICAL TUBE |
| 00192896093430 | TUBE SHAFT WITH LUER LOCK INSULATED |
| 00192896103627 | Tube Shaft Insulated With Luer Lock |
| 00192896110472 | Tube Shaft Diameter 5 Millimeter, Insulated Without Luer Lock |
| 00192896110465 | Tube Shaft Diameter 5 Millimeter, Insulated Without Luer Lock |
| 00192896111912 | Tube Shaft/Insulated Cylindrical Without Luer Lock |