| Primary Device ID | 06945121410090 |
| NIH Device Record Key | e2afcc44-792c-4e61-a610-4e7f62cd8dcf |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Phased probe |
| Version Model Number | P3-E |
| Company DUNS | 544914187 |
| Company Name | CHISON Medical Technologies 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 | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06945121409773 [Primary] |
| GS1 | 06945121410090 [Package] Contains: 06945121409773 Package: [1 Units] In Commercial Distribution |
| GS1 | 06945121410823 [Package] Contains: 06945121409773 Package: [2 Units] In Commercial Distribution |
| ITX | Transducer, Ultrasonic, Diagnostic |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 4 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2016-09-24 |
| 06945121412377 | D5P64L |
| 06945121412360 | D3P64LS |
| 06945121410274 | P2-ES |
| 06945121410106 | P6-E |
| 06945121410090 | P3-E |
| 06945121410083 | P2-E |