| Primary Device ID | 30705036003971 |
| NIH Device Record Key | e53d5591-628b-41e7-8ded-5f26c75eba2c |
| Commercial Distribution Discontinuation | 2020-04-13 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | N/A |
| Version Model Number | RGCT180 |
| Catalog Number | RGCT180 |
| Company DUNS | 486911852 |
| Company Name | Obtech Medical Sàrl |
| 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 | true |
| OTC Over-The-Counter | false |
| Phone | +1(877)384-4266 |
| customersupport@eesus.jnj.com | |
| Phone | +1(877)384-4266 |
| customersupport@eesus.jnj.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 20705036003974 [Primary] |
| GS1 | 30705036003971 [Package] Contains: 20705036003974 Package: CASE [42 Units] Discontinued: 2020-04-13 Not in Commercial Distribution |
| KNT | TUBES, GASTROINTESTINAL (AND ACCESSORIES) |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2020-04-14 |
| Device Publish Date | 2016-07-15 |
| 30705036011792 | Huber Needle |
| 30705036011785 | Huber Needle |
| 30705036003988 | Gastric Calibration Tube |
| 30705036003971 | Gastric Calibration Tube |
| 30705036003964 | Gastric Band Dissector |