| Primary Device ID | 00192896027923 |
| NIH Device Record Key | 88077835-45f7-410e-9886-6253753c9af7 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | STILLE-LISTON BONE CUTTING FORCEPS |
| Version Model Number | 315-756 |
| Catalog Number | 315-756 |
| 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 |
| Length | 10.5 Inch |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00192896027923 [Primary] |
| HTZ | INSTRUMENT, CUTTING, ORTHOPEDIC |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00192896027923]
Moist Heat or Steam Sterilization;Dry Heat Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2019-07-12 |
| Device Publish Date | 2018-09-13 |
| 00192896027923 | STILLE-LISTON BONE CUTTING FORCEPS DOUBLE ACTION ANGLED JAW |
| 00192896027916 | STILLE-LISTON BONE CUTTING FORCEPS DOUBLE ACTION STRAIGHT JAW |
| 00192896027909 | STILLE-LISTON BONE CUTTING FORCEPS DOUBLE ACTION UP-ANGLE JAW |
| 00192896101272 | STILLE-LISTON BONE CUTTING FORCEPS DOUBLE CROSSED UP-ANGLE TIP |