| Primary Device ID | 05712149000777 |
| NIH Device Record Key | ce7f6c54-d3ef-4de7-a478-8eba7d66e224 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Oticon Medical |
| Version Model Number | M50504 |
| Catalog Number | M50504 |
| Company DUNS | 554563994 |
| Company Name | Oticon Medical AB |
| 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 | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | false |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Phone | 888-277-8014 |
| info@oticonmedical.com | |
| Phone | 888-277-8014 |
| info@oticonmedical.com | |
| Phone | 888-277-8014 |
| info@oticonmedical.com | |
| Phone | 888-277-8014 |
| info@oticonmedical.com | |
| Phone | 888-277-8014 |
| info@oticonmedical.com | |
| Phone | 888-277-8014 |
| info@oticonmedical.com | |
| Phone | 888-277-8014 |
| info@oticonmedical.com | |
| Phone | 888-277-8014 |
| info@oticonmedical.com | |
| Phone | 888-277-8014 |
| info@oticonmedical.com | |
| Phone | 888-277-8014 |
| info@oticonmedical.com | |
| Phone | 888-277-8014 |
| info@oticonmedical.com | |
| Phone | 888-277-8014 |
| info@oticonmedical.com | |
| Phone | 888-277-8014 |
| info@oticonmedical.com | |
| Phone | 888-277-8014 |
| info@oticonmedical.com | |
| Phone | 888-277-8014 |
| info@oticonmedical.com | |
| Phone | 888-277-8014 |
| info@oticonmedical.com | |
| Phone | 888-277-8014 |
| info@oticonmedical.com | |
| Phone | 888-277-8014 |
| info@oticonmedical.com | |
| Phone | 888-277-8014 |
| info@oticonmedical.com |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 05712149000777 [Primary] |
| LXB | Hearing Aid, Bone Conduction |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2018-10-22 |
| Device Publish Date | 2016-09-09 |
| 05712149008872 | Double-ended Dissector |
| 05712149008865 | Ruler |
| 05712149008285 | Sterilization cassette |
| 05712149000777 | Genie Medical fitting software |