| Primary Device ID | 00813307014430 |
| NIH Device Record Key | 5f9e4a92-b0e6-4b17-9ca9-37f98ce1d58e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | InHealth Technologies; Blom-Singer |
| Version Model Number | IN 2008-LETO |
| 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 |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry; Keep Away From Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry; Keep Away From Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry; Keep Away From Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry; Keep Away From Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry; Keep Away From Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry; Keep Away From Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry; Keep Away From Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry; Keep Away From Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry; Keep Away From Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry; Keep Away From Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry; Keep Away From Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry; Keep Away From Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry; Keep Away From Sunlight |
| Special Storage Condition, Specify | Between 0 and 0 *Keep Dry; Keep Away From Sunlight |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00813307014430 [Primary] |
| EWL | Prosthesis, Laryngeal (Taub) |
| 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 |