| Primary Device ID | 38809407786608 |
| NIH Device Record Key | 548e9e42-43f7-4149-ba5c-7016bc0e784e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ELASTY Mesoneedle 32Gx8mm |
| Version Model Number | FDN 53 |
| Company DUNS | 688432407 |
| Company Name | Feeltech 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 | false |
| Expiration Date | true |
| 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 | 08809407786607 [Unit of Use] |
| GS1 | 18809407786604 [Primary] |
| GS1 | 28809407786601 [Package] Contains: 18809407786604 Package: [1000 Units] In Commercial Distribution |
| GS1 | 38809407786608 [Package] Contains: 28809407786601 Package: [5000 Units] In Commercial Distribution |
| FMI | Needle, Hypodermic, Single Lumen |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2019-11-13 |
| Device Publish Date | 2019-11-05 |