| Primary Device ID | 00192896056053 |
| NIH Device Record Key | 108a6ac1-57df-4dce-be93-e9dee7574c51 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | JOSEPH PECK SCISSORS |
| Version Model Number | 1200-945 |
| Catalog Number | 1200-945 |
| Company DUNS | 040729840 |
| Company Name | SONTEC INSTRUMENTS, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| MRI Safety Status | Labeling does n |
| 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 | 6 Inch |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00192896056053 [Primary] |
| LRW | SCISSORS, GENERAL, SURGICAL |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00192896056053]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-12-21 |
| Device Publish Date | 2018-09-27 |
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