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 |