| Primary Device ID | 04580406860720 | 
| NIH Device Record Key | 121ff214-1b61-45af-9a0f-b4310525bfa2 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | AP set 7 | 
| Version Model Number | AP set 7 | 
| Catalog Number | 50796 | 
| Company DUNS | 690713813 | 
| Company Name | OSADA ELECTRIC CO.,LTD. | 
| 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 | true | 
| 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 | 04580406860720 [Primary] | 
| ELC | Scaler, ultrasonic | 
| Steralize Prior To Use | true | 
| Device Is Sterile | false | 
[04580406860720]
Moist Heat or Steam Sterilization
| Public Version Status | Update | 
| Device Record Status | Published | 
| Public Version Number | 4 | 
| Public Version Date | 2019-02-21 | 
| Device Publish Date | 2016-09-20 | 
| 04582227353498 - ST45 | 2020-03-27 | 
| 04580406860690 - ST38-90R | 2019-02-21 | 
| 04580406860706 - ST38-90L | 2019-02-21 | 
| 04580406860713 - ST38-90 | 2019-02-21 | 
| 04580406860720 - AP set 7 | 2019-02-21 | 
| 04580406860720 - AP set 7 | 2019-02-21 | 
| 04580406860737 - AP point 1 | 2019-02-21 | 
| 04580406860744 - AP point 2 | 2019-02-21 | 
| 04580406860751 - AP point 3 | 2019-02-21 |