| Primary Device ID | 00192896025714 |
| NIH Device Record Key | 50915681-7ee8-4864-9bd1-6f51f9ca96d1 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | WALTER AUFRICHT NASAL RETRACTOR |
| Version Model Number | 207-2928 |
| Catalog Number | 207-2928 |
| 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 | 5.25 Inch |
| Length | 5.25 Inch |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00192896025714 [Primary] |
| KAL | RETRACTOR, ENT |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00192896025714]
Dry Heat Sterilization;Moist Heat or Steam Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-10-12 |
| Device Publish Date | 2018-09-11 |
| 00192896025714 | WALTER AUFRICHT NASAL RETRACTOR DOUBLE ENDED |
| 00192896025707 | WALTER AUFRICHT NASAL RETRACTOR DOUBLE ENDED |
| 00192896098725 | WALTER AUFRICHT NASAL RETRACTOR DOUBLE ENDED BLUNT BLADE |
| 00192896117877 | Walter Aufricht Nasal Retractor Double Ended Illuminated 60 Millimeter x 4 Millimeter Long Tip |
| 00192896117860 | Walter Aufricht Nasal Retractor Double Ended 60 Millimeter x 4 Millimeter Long Tip |
| 00192896119895 | Walter Aufricht Nasal Retractor Double End Without Prongs Titanium |
| 00192896119888 | Walter Aufricht Nasal Retractor Double End Without Prongs |