| Primary Device ID | 00811907030522 |
| NIH Device Record Key | d3fd579d-cbaa-4c7f-838a-a60c34024126 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Zephyr Delivery Catheter |
| Version Model Number | EDC-TS-4.0 |
| Company DUNS | 958582595 |
| Company Name | PULMONX CORPORATION |
| Device Count | 1 |
| DM Exempt | false |
| 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 |
| Phone | 866-300-4550 |
| USCustomerService@pulmonx.com | |
| Phone | 866-300-4550 |
| USCustomerService@pulmonx.com |
| Device Size Text, specify | 0 |
| Device Size Text, specify | 0 |
| Handling Environment Temperature | Between -18 Degrees Celsius and 60 Degrees Celsius |
| Handling Environment Temperature | Between -18 Degrees Celsius and 60 Degrees Celsius |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00811907030522 [Primary] |
| NJK | Valve, Pulmonary |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2018-08-20 |
| Device Publish Date | 2018-07-20 |
| 00811907030720 | The Zephyr® Endobronchial Valve (Zephyr Valve) is an endobronchial implant designed to occlude |
| 00811907030621 | The Zephyr® Endobronchial Valve (Zephyr Valve) is an endobronchial implant designed to occlude |
| 00811907030522 | The Zephyr® Endobronchial Valve (Zephyr Valve) is an endobronchial implant designed to occlude |
| 00811907031222 | The Zephyr® Endobronchial Valve (Zephyr Valve) is an endobronchial implant designed to occlude |