Primary Device ID | 00811907030621 |
NIH Device Record Key | ae23d440-6b70-46cb-92bd-7cc4a2d177e2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Zephyr Delivery Catheter |
Version Model Number | EDC-TS-4.0-J |
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 | 00811907030621 [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 |