Primary Device ID | 06973493599860 |
NIH Device Record Key | 50140dbe-d306-4728-ac99-122ef8c63b57 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Goldeep |
Version Model Number | S12 |
Company DUNS | 403304567 |
Company Name | Shenzhen TPH Technology 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 | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06973493598016 [Primary] |
GS1 | 06973493599860 [Package] Contains: 06973493598016 Package: carton [24 Units] In Commercial Distribution |
HGX | Pump, Breast, Powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-08-16 |
Device Publish Date | 2022-08-08 |
06973493599860 | S12 |
06973493590317 | S12-D |
06973493594179 | S12-D |
06973493599198 | S12-D |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
GOLDEEP 90108813 not registered Live/Pending |
Gong, Lifen 2020-08-12 |