| Primary Device ID | 10841470103191 | 
| NIH Device Record Key | e11cb9cd-def6-4e81-ae7d-b773a378d443 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Blom | 
| Version Model Number | 313-10-080 | 
| 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 | 00841470103194 [Primary] | 
| GS1 | 10841470103191 [Package] Contains: 00841470103194 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 |