| Primary Device ID | 20681490138639 |
| NIH Device Record Key | abcb7d48-a17d-4184-8617-f56561778ce9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | BRIDGEMASTER® |
| Version Model Number | 600306 |
| Company DUNS | 835465063 |
| Company Name | MEDTRONIC XOMED, INC. |
| Device Count | 1 |
| DM Exempt | false |
| Pre-market Exempt | true |
| 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 | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00681490138635 [Primary] |
| GS1 | 20681490138639 [Package] Contains: 00681490138635 Package: PK [5 Units] In Commercial Distribution |
| EPP | SPLINT, NASAL |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 3 |
| Public Version Date | 2019-05-23 |
| Device Publish Date | 2017-09-09 |
| 20681490138639 | SPLINT 600306 BRIDGEMASTER 5PK LARGE |
| 20681490138622 | SPLINT 600302 BRIDGEMASTER 5PK SMALL |