Primary Device ID | 05030267160525 |
NIH Device Record Key | f94ded5b-014f-4024-b1d4-d0def649bf08 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | PULMO-PROTECT LUNG FUNCTION FILTER |
Version Model Number | 1691003 |
Company DUNS | 785952607 |
Company Name | Intersurgical Incorporated |
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 | true |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 3154512900 |
support@intersurgicalinc.com | |
Phone | 3154512900 |
support@intersurgicalinc.com | |
Phone | 3154512900 |
support@intersurgicalinc.com | |
Phone | 3154512900 |
support@intersurgicalinc.com | |
Phone | 3154512900 |
support@intersurgicalinc.com | |
Phone | 3154512900 |
support@intersurgicalinc.com | |
Phone | 3154512900 |
support@intersurgicalinc.com | |
Phone | 3154512900 |
support@intersurgicalinc.com | |
Phone | 3154512900 |
support@intersurgicalinc.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 05030267156054 [Primary] |
GS1 | 05030267160525 [Package] Contains: 05030267156054 Package: [50 Units] In Commercial Distribution |
BZG | Spirometer, Diagnostic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2022-07-25 |
Device Publish Date | 2022-07-15 |
05030267160525 | PULMO-PROTECT LUNG FUNCTION FILTER |
05030267135998 | PULMO-PROTECT LUNG FUNCTION FILTER |