Primary Device ID | 06945121410106 |
NIH Device Record Key | c7ac416a-97dc-4d08-9b16-10cabf12b279 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Phased probe |
Version Model Number | P6-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 | 06945121409780 [Primary] |
GS1 | 06945121410106 [Package] Contains: 06945121409780 Package: [1 Units] In Commercial Distribution |
GS1 | 06945121412001 [Package] Contains: 06945121409780 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 |