Primary Device ID | 10841470100817 |
NIH Device Record Key | 850c0b07-565d-4328-8b77-acffaacfcbcf |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | VT Select |
Version Model Number | 313-5594 |
Company DUNS | 030619483 |
Company Name | PULMODYNE 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 | 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 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841470100810 [Primary] |
GS1 | 10841470100817 [Package] Contains: 00841470100810 Package: [8 Units] In Commercial Distribution |
BTM | Ventilator, Emergency, Manual (Resuscitator) |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2023-04-18 |
Device Publish Date | 2023-04-10 |
10841470100817 | 313-5594 |
10841470100794 | 313-5593 |
10841470100770 | 313-5591 |
10841470100749 | 313-5592 |
10841470100718 | 313-5590 |