| Primary Device ID | 06970399639690 |
| NIH Device Record Key | acce9bde-fa94-4e88-9498-b7c21efe209c |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | AccuBlade |
| Version Model Number | 800200900 |
| Company DUNS | 560430218 |
| Company Name | Hangzhou Rejoin Mastin Medical Device Co., Ltd. |
| 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 | true |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | true |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | false |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06970399639690 [Primary] |
| HTT | Burr, Orthopedic |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-05-26 |
| Device Publish Date | 2023-05-18 |
| 06972884984698 | Blade 4.2 Toothless,SN_5 |
| 06972884984681 | Blade 4.2 Double Edge,SN_5 |
| 06970399639690 | Blade 4.2 Power Double Double Edge,SN_5 |
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
![]() ACCUBLADE 85034310 4068101 Live/Registered |
EDGEWELL PERSONAL CARE BRANDS, LLC 2010-05-10 |
![]() ACCUBLADE 79006213 3006071 Dead/Cancelled |
YONEX KABUSHIKI KAISHA 2004-09-03 |