| Primary Device ID | 06971119542009 | 
| NIH Device Record Key | fd8a7567-22bf-4509-9721-1dfc3660727a | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Saw blade | 
| Version Model Number | HF113040HP | 
| Company DUNS | 543260808 | 
| Company Name | Guangdong JINME Medical Technology 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 | false | 
| Lot Batch | false | 
| Serial Number | true | 
| Manufacturing Date | true | 
| 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 | 06971119542009 [Primary] | 
| GFA | Blade, Saw, General & Plastic Surgery, Surgical | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2025-07-23 | 
| Device Publish Date | 2025-07-15 | 
| 06971119542016 | Saw blade | 
| 06971119542009 | Saw blade | 
| 06971119541996 | Saw blade | 
| 06971119541989 | Saw blade | 
| 06971119541972 | Saw blade | 
| 06971119541965 | Saw blade | 
| 06971119541958 | Saw blade | 
| 06971119541941 | Saw blade | 
| 06971119541934 | Saw blade | 
| 06971119541927 | Saw blade | 
Mark Image Registration | Serial  | Company  Trademark Application Date  | 
|---|---|
![]() SAW BLADE  86743338  not registered Dead/Abandoned  | 
        Renehan, Andrew  2015-09-01  | 
![]() SAW BLADE  85439083  4350902 Live/Registered  | 
        Spin Master Ltd.  2011-10-04  |