| Primary Device ID | 10868750000247 |
| NIH Device Record Key | 62549ff0-3082-4f8e-969c-9696ca12b05f |
| Commercial Distribution Discontinuation | 2019-10-17 |
| Commercial Distribution Status | Not in Commercial Distribution |
| Brand Name | Pulmonary Filtration Technologies |
| Version Model Number | 7700PFT |
| Catalog Number | 7700PFT |
| Company DUNS | 058027090 |
| Company Name | WHITE CARDIOPULMONARY, 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 | true |
| Expiration Date | false |
| 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 |
|---|---|
| GS1 | 10868750000247 [Primary] |
| BZG | Spirometer, Diagnostic |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-11-06 |
| Device Publish Date | 2016-09-21 |
| 10868750000230 | 10868750000230 = basePkg; 20868750000237 = higherPkg1 - contains 100 of the base package Primary |
| 10868750000247 | 10868750000247 = basePkg; 20868750000244 = higherPkg1 - contains 100 of the base package Primary |
| 10868750000223 | 10868750000223 = basePkg; 20868750000220 = higherPkg1 - contains 100 of the base package Primary |
| 10868750000216 | 10868750000216 = basePkg; 20868750000213 = higherPkg1 - contains 100 of the base package Primary |