| Primary Device ID | 00636266958351 |
| NIH Device Record Key | 7ef36760-6896-45ab-8fa8-50430415df29 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Sonus M 2 Tip |
| Version Model Number | M 2 |
| Catalog Number | 133-1202 |
| Company DUNS | 002965168 |
| Company Name | ENGLER ENGINEERING CORPORATION |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | true |
| MRI Safety Status | MR Unsafe |
| 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 | false |
| OTC Over-The-Counter | true |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00636266958351 [Primary] |
| ELC | Scaler, Ultrasonic |
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00636266958351]
Liquid Chemical;Dry Heat Sterilization
[00636266958351]
Liquid Chemical;Dry Heat Sterilization
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-08-16 |
| Device Publish Date | 2018-07-16 |
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