Primary Device ID | 10841470103320 |
NIH Device Record Key | e07a33ca-a718-4e98-811e-82f9738553aa |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Blom |
Version Model Number | 313-13-060 |
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 |
Phone | 317-246-5505 |
info@pulmodyne.com |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841470103323 [Primary] |
GS1 | 10841470103320 [Package] Contains: 00841470103323 Package: [10 Units] In Commercial Distribution |
BTO | Tube, Tracheostomy (W/Wo Connector) |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2015-11-13 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
BLOM 87664164 5485901 Live/Registered |
BLOM Limited Corporation 2017-10-30 |
BLOM 86781621 5152126 Live/Registered |
BLOM Limited 2015-10-08 |
BLOM 86348617 4707669 Live/Registered |
Hansa Medical Products, Inc. 2014-07-25 |
BLOM 77282240 3610558 Dead/Cancelled |
Hansa Medical Products, Inc. 2007-09-18 |