Primary Device ID | 10868750000216 |
NIH Device Record Key | 2e3c8b0e-87f3-4f49-9240-06eccefab73f |
Commercial Distribution Discontinuation | 2019-11-27 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | Pulmonary Filtration Technologies |
Version Model Number | 7400PFT |
Catalog Number | 7400PFT |
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 | 10868750000216 [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 | 2019-12-05 |
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 |