| Primary Device ID | 06923646508676 |
| NIH Device Record Key | 38d6bcc6-0deb-4c16-be2e-b1453a491215 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Ligation Device |
| Version Model Number | Loop15B0-LD195D0 |
| Catalog Number | Loop15B0-LD195D0 |
| Company DUNS | 421371962 |
| Company Name | Leo Medical 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 | 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 | 06923646508676 [Primary] |
| FHN | Ligator, Hemorrhoidal |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2026-01-12 |
| Device Publish Date | 2026-01-04 |
| 06923646508737 | Loop30B0-LD230D0 |
| 06923646508638 | Loop15B0-LD165D0 |
| 06923646508744 | Loop40B0-LD230D0 |
| 06923646508720 | Loop20B0-LD230D0 |
| 06923646508713 | Loop15B0-LD230D0 |
| 06923646508706 | Loop40B0-LD195D0 |
| 06923646508690 | Loop30B0-LD195D0 |
| 06923646508683 | Loop20B0-LD195D0 |
| 06923646508676 | Loop15B0-LD195D0 |
| 06923646508669 | Loop40B0-LD165D0 |
| 06923646508652 | Loop30B0-LD165D0 |
| 06923646508645 | Loop20B0-LD165D0 |