| Primary Device ID | B504OMGS9021500320 |
| NIH Device Record Key | 54cc6b4b-967b-4721-b3aa-50c51ef54244 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Brasseler |
| Version Model Number | GS902.150.032 |
| Company DUNS | 016889401 |
| Company Name | Provision |
| 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 | true |
| 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 |
| Device Issuing Agency | Device ID |
|---|---|
| HIBCC | B504OMGS9021500320 [Primary] |
| LXH | Orthopedic Manual Surgical Instrument |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-01-26 |
| Device Publish Date | 2022-01-18 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() BRASSELER 76138861 not registered Dead/Abandoned |
Gebr. Brasseler Gmbh & Co. KG 2000-09-29 |
![]() BRASSELER 72072698 0706436 Live/Registered |
Brasseler; Peter 1959-05-01 |