| Primary Device ID | 17290018632144 |
| NIH Device Record Key | 66f7cceb-7c73-4796-b022-4366e527419f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Replaceable Inner Tubes |
| Version Model Number | FG-20F-GREEN-REP |
| Catalog Number | FG-20F-GREEN-REP |
| Company DUNS | 600363369 |
| Company Name | FIDMI MEDICAL LTD |
| Device Count | 5 |
| DM Exempt | false |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | true |
| 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 | 07290018632147 [Primary] |
| GS1 | 17290018632144 [Unit of Use] |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2021-08-23 |
| Device Publish Date | 2021-08-15 |
| 07290018632154 | The Replacement Feeding Tube is designed to be replaced when needed. It is attached to the place |
| 17290018632144 | The Replacement Feeding Tube is designed to be replaced when needed. It is attached to the place |
| 17290018632137 | The Replacement Feeding Tube is designed to be replaced when needed. It is attached to the place |
| 17290018632120 | The Replacement Feeding Tube is designed to be replaced when needed. It is attached to the place |
| 17290018632113 | The Replacement Feeding Tube is designed to be replaced when needed. It is attached to the place |