| Primary Device ID | 10811955020299 |
| NIH Device Record Key | 03627f56-43cb-4f47-9fec-9cbf9d5c6fd9 |
| Commercial Distribution Discontinuation | 2021-12-17 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | RapidPort EZ |
| Version Model Number | C-2306 |
| Catalog Number | C-2306 |
| Company DUNS | 625064352 |
| Company Name | Apollo Endosurgery, Inc. |
| 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 | true |
| Device Combination Product | false |
| Single Use | true |
| Lot Batch | true |
| Serial Number | true |
| Manufacturing Date | false |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | true |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 855-551-3123 |
| productcomplaints.us@apolloendo.com | |
| Phone | 855-551-3123 |
| productcomplaints.us@apolloendo.com | |
| Phone | 855-551-3123 |
| productcomplaints.us@apolloendo.com | |
| Phone | 855-551-3123 |
| productcomplaints.us@apolloendo.com | |
| Phone | 855-551-3123 |
| productcomplaints.us@apolloendo.com | |
| Phone | 855-551-3123 |
| productcomplaints.us@apolloendo.com | |
| Phone | 855-551-3123 |
| productcomplaints.us@apolloendo.com | |
| Phone | 855-551-3123 |
| productcomplaints.us@apolloendo.com | |
| Phone | 855-551-3123 |
| productcomplaints.us@apolloendo.com | |
| Phone | 855-551-3123 |
| productcomplaints.us@apolloendo.com | |
| Phone | 855-551-3123 |
| productcomplaints.us@apolloendo.com | |
| Phone | 855-551-3123 |
| productcomplaints.us@apolloendo.com | |
| Phone | 855-551-3123 |
| productcomplaints.us@apolloendo.com | |
| Phone | 855-551-3123 |
| productcomplaints.us@apolloendo.com | |
| Phone | 855-551-3123 |
| productcomplaints.us@apolloendo.com | |
| Phone | 855-551-3123 |
| productcomplaints.us@apolloendo.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 10811955020299 [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 | 5 |
| Public Version Date | 2021-12-30 |
| Device Publish Date | 2016-08-12 |
| 10811955020299 | RapidPort EZ Access Port Kit |
| 10811955020282 | RapidPort EZ Access Port Kit |
| 10811955020053 | RapidPort EZ Applier Tool |