| Primary Device ID | 06970908212932 |
| NIH Device Record Key | e64107a8-dcfa-4241-8975-a6d951bd828f |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Esperance 3+ Aspiration Catheter System |
| Version Model Number | ASP3F160KIT |
| Company DUNS | 544535295 |
| Company Name | Shanghai Wallaby Medical Technologies Co., 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 | 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 | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06970908212932 [Primary] |
| NRY | Catheter, Thrombus Retriever |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-11-19 |
| Device Publish Date | 2024-11-11 |
| 06970908213625 | The Esperance® 3+ Aspiration Catheter is a single-use, vascular catheter consisting of a single |
| 06970908212932 | The Esperance® 3+ Aspiration Catheter is a single-use, vascular catheter consisting of a single |
| 06970908212925 | The Esperance® 3+ Aspiration Catheter is a single-use, vascular catheter consisting of a single |
| 06970908212918 | The Esperance® 3+ Aspiration Catheter is a single-use, vascular catheter consisting of a single |
| 06970908212901 | The Esperance® 3+ Aspiration Catheter is a single-use, vascular catheter consisting of a single |