Primary Device ID | 26973163403118 |
NIH Device Record Key | 050eb8b9-9da8-454c-9b3b-66fef442252f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | KINGFA MEDICAL |
Version Model Number | KG-1802 |
Company DUNS | 543265548 |
Company Name | Guangdong KINGFA SCI.&TECH. Co., Ltd. |
Device Count | 100 |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | true |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 06973163403114 [Unit of Use] |
GS1 | 16973163403111 [Primary] |
GS1 | 26973163403118 [Package] Contains: 16973163403111 Package: carton [10 Units] In Commercial Distribution |
LZA | Polymer Patient Examination Glove |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2021-05-18 |
Device Publish Date | 2021-05-10 |
26973163403231 | Extra large size |
26973163403224 | Large size |
26973163403217 | Medium size |
26973163403200 | Small size |
26973163403118 | Extra large size |
26973163403101 | Large size |
26973163403095 | Medium size |
26973163403088 | Small size |
26973163402968 | Extra large size |
26973163402951 | Large size |
26973163402944 | Medium size |
06973163402933 | Small size |
06973163404197 | KF-A F02(N) |
06973163406184 | KF-B P05(L3) |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
KINGFA MEDICAL 90352238 not registered Live/Pending |
KINGFA SCI.&TECH.CO.,LTD 2020-12-01 |