| Primary Device ID | 38809407786172 |
| NIH Device Record Key | 8d49a3df-b99a-40bf-bc99-0acbf5a1879b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Miracu BI |
| Version Model Number | Miracu BI 23Gx60mm |
| Company DUNS | 688432407 |
| Company Name | Feeltech Co.,Ltd. |
| Device Count | 10 |
| 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 | 08809407786171 [Unit of Use] |
| GS1 | 18809407786178 [Primary] |
| GS1 | 28809407786175 [Package] Contains: 18809407786178 Package: [10 Units] In Commercial Distribution |
| GS1 | 38809407786172 [Package] Contains: 28809407786175 Package: [300 Units] In Commercial Distribution |
| NEW | Suture, Surgical, Absorbable, Polydioxanone |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2021-02-05 |
| Device Publish Date | 2019-09-01 |
| 38809407786189 | Miracu BI 23Gx90mm |
| 38809407786172 | Miracu BI 23Gx60mm |
| 38809407786165 | Miracu BI 21Gx60mm |