| Primary Device ID | B09920942500 |
| NIH Device Record Key | fa134669-5d3c-49f2-8cae-b6a9b947bc82 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | MICTEC PLEURA ABRADER |
| Version Model Number | 20942-50 |
| 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 | 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 | 800-821-7496 |
| info@sontecinstruments.com | |
| Phone | 800-821-7496 |
| info@sontecinstruments.com | |
| Phone | 800-821-7496 |
| info@sontecinstruments.com |
| Length | 300 Millimeter |
| Length | 300 Millimeter |
| Length | 300 Millimeter |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00192896008793 [Primary] |
| HIBCC | B09920942500 [Previous] |
| GCJ | Laparoscope, General & Plastic Surgery |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[B09920942500]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[B09920942500]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
[B09920942500]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-09-24 |
| Device Publish Date | 2018-08-24 |
| B09920942510 | MICTEC PLEURA ABRADER CYLINDER STYLE |
| B09920942500 | MICTEC PLEURA ABRADER BALL STYLE ANGLED DOWN |