| Primary Device ID | 00813307014713 |
| NIH Device Record Key | 5ab94d99-d8c3-42c5-a0e5-1d97f78401d3 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | InHealth Technologies; Blom-Singer; Dual Valve |
| Version Model Number | DV 2006-NS |
| Company DUNS | 120981337 |
| Company Name | Freudenberg Medical, LLC |
| 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 | true |
| 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 | 800-477-5969 |
| InHealth@inhealth.com | |
| Phone | 800-477-5969 |
| InHealth@inhealth.com | |
| Phone | 800-477-5969 |
| InHealth@inhealth.com | |
| Phone | 800-477-5969 |
| InHealth@inhealth.com | |
| Phone | 800-477-5969 |
| InHealth@inhealth.com | |
| Phone | 800-477-5969 |
| InHealth@inhealth.com | |
| Phone | 800-477-5969 |
| InHealth@inhealth.com | |
| Phone | 800-477-5969 |
| InHealth@inhealth.com | |
| Phone | 800-477-5969 |
| InHealth@inhealth.com | |
| Phone | 800-477-5969 |
| InHealth@inhealth.com | |
| Phone | 800-477-5969 |
| InHealth@inhealth.com | |
| Phone | 800-477-5969 |
| InHealth@inhealth.com | |
| Phone | 800-477-5969 |
| InHealth@inhealth.com | |
| Phone | 800-477-5969 |
| InHealth@inhealth.com | |
| Phone | 800-477-5969 |
| InHealth@inhealth.com | |
| Phone | 800-477-5969 |
| InHealth@inhealth.com | |
| Phone | 800-477-5969 |
| InHealth@inhealth.com |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Special Storage Condition, Specify | Between 0 and 0 *Keep away from sunlight; Keep dry |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00813307014713 [Primary] |
| EPE | Brush, Cleaning, Tracheal Tube |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 2 |
| Public Version Date | 2018-03-29 |
| Device Publish Date | 2018-01-01 |
| 00813307014713 | DV 2006-NS |
| 00813307010975 | DV 2014-NS |
| 00813307010968 | DV 2012-NS |
| 00813307010951 | DV 2010-NS |
| 00813307010944 | DV 2008-NS |
| 00848253001517 | DV 2014-LF |
| 00848253001500 | DV 2012-LF |
| 00848253001494 | DV 2010-LF |
| 00848253001487 | DV 2008-LF |
| 00848253001470 | DV 2006-LF |