Primary Device ID | 06972884984681 |
NIH Device Record Key | 61a08c6b-1ccf-45e4-885a-45d02e2da6f9 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AccuBlade |
Version Model Number | 800200100 |
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 | 06972884984681 [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 |