Primary Device ID | 44710810117396 |
NIH Device Record Key | 450f69e2-6197-4609-b47e-e47725e6ff5c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Venti.Plus |
Version Model Number | H100 |
Catalog Number | Hyperinflation System 1.0L |
Company DUNS | 656854379 |
Company Name | GALEMED CORPORATION |
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 | 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 Issuing Agency | Device ID |
---|---|
GS1 | 04710810117398 [Primary] |
GS1 | 44710810117396 [Package] Contains: 04710810117398 Package: Carton [20 Units] In Commercial Distribution |
NHK | Resuscitator,Manual,Non Self-Inflating |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-09-24 |
44710810117396 | H100 |
44710810117389 | H050 |
44710810117372 | H025 |
44710810100503 | H100-M |
44710810100497 | H050-M |
44710810100480 | H025-M |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
VENTI.PLUS 77881643 not registered Dead/Abandoned |
GALEMED CORPORATION 2009-11-28 |
VENTI.PLUS 77645179 not registered Dead/Abandoned |
GALEMED CORPORATION 2009-01-07 |