Primary Device ID | 06951740502085 |
NIH Device Record Key | aac9dd3f-ad62-4c08-8e3e-ac6d01c5cf2a |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | HYLOGY |
Version Model Number | JPD--100S6 |
Company DUNS | 529217911 |
Company Name | Shenzhen Jumper Medical Equipment 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 | true |
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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06951740502085 [Primary] |
KNG | Monitor, Ultrasonic, Fetal |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-05-19 |
06951740505215 | JPD-FR401 |
06951740502085 | JPD--100S6 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
HYLOGY 87577585 5401698 Live/Registered |
SHENZHEN DAJIE TECHNOLOGY CO., LTD. 2017-08-21 |