| Primary Device ID | B001RSM2101 |
| NIH Device Record Key | 62f9a69e-3ef8-4e0f-a283-d21464ca9e8b |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ReShape™ Removal Catheter |
| Version Model Number | RSM210 |
| Catalog Number | RSM210 |
| Company DUNS | 877283486 |
| Company Name | RESHAPE MEDICAL, INC. |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | false |
| MRI Safety Status | MR Unsafe |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B001RSM2101 [Primary] |
| LTI | Implant, Intragastric For Morbid Obesity |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-07-06 |
| Device Publish Date | 2015-08-25 |
| B001RSM1011 - ReShape™ Integrated Dual Balloon System | 2018-07-06 IMPLANT, INTRAGASTRIC BALLOON FOR OBESITY |
| B001RSM1101 - ReShape® Integrated Dual Balloon System | 2018-07-06 IMPLANT, INTRAGASTRIC BALLOON FOR OBESITY |
| B001RSM2101 - ReShape™ Removal Catheter | 2018-07-06ReShape™ Removal Catheter - component to remove the ReShape™ Integrated Dual Balloon |
| B001RSM2101 - ReShape™ Removal Catheter | 2018-07-06 ReShape™ Removal Catheter - component to remove the ReShape™ Integrated Dual Balloon |
| B001RSM9001 - ReShape™ Valve Sealant | 2018-07-06 ReShape™ Valve Sealant - component for use with the ReShape™ Integrated Dual Balloon |