Primary Device ID | 06951740517959 |
NIH Device Record Key | c296e470-ff26-4e81-8f5b-1b2b04cb60aa |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PUREMED |
Version Model Number | JPD-HA200C |
Company DUNS | 529217911 |
Company Name | Shenzhen Jumper Medical Equipment Co.,Ltd. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | true |
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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06951740517959 [Primary] |
DXN | System, Measurement, Blood-Pressure, Non-Invasive |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-12-12 |
Device Publish Date | 2023-12-04 |
06951740590112 - JUMPER | 2024-08-12 |
06951740500388 - JUMPER | 2024-07-25 |
06951740520256 - JUMPER | 2024-07-25 |
06951740520263 - JUMPER | 2024-07-25 |
06951740520270 - JUMPER | 2024-07-25 |
06951740520287 - JUMPER | 2024-07-25 |
06951740520294 - JUMPER | 2024-07-25 |
06951740520300 - JUMPER | 2024-07-25 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
PUREMED 98721123 not registered Live/Pending |
SPIELBERG, MAX 2024-08-28 |
PUREMED 88725881 not registered Live/Pending |
SHENZHEN EJ TECHNOLOGY CO., LTD 2019-12-13 |
PUREMED 77201723 3772049 Live/Registered |
Georgia Gulf Corporation 2007-06-08 |