| Primary Device ID | 26973163403231 |
| NIH Device Record Key | 737dd142-06e5-432a-8134-6e7f26bd39c0 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | KINGFA MEDICAL |
| Version Model Number | KG-1601 |
| 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 | 06973163403237 [Unit of Use] |
| GS1 | 16973163403234 [Primary] |
| GS1 | 26973163403231 [Package] Contains: 16973163403234 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 |