Primary Device ID | 06951740501644 |
NIH Device Record Key | d14ad772-9068-4627-8fa4-810a7e52fb02 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Morpilot |
Version Model Number | JPD-FR401 |
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 | 06951740501644 [Primary] |
FLL | Thermometer, Electronic, Clinical |
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 |
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 |
---|---|
MORPILOT 98266766 not registered Live/Pending |
Keenstone Corp. 2023-11-13 |
MORPILOT 86849774 5098791 Live/Registered |
Keenstone Corp. 2015-12-15 |