| Primary Device ID | 06944749500305 | 
| NIH Device Record Key | 64fbcb4f-53c8-4997-8835-7bd85ff56a60 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | YHMED | 
| Version Model Number | QDC-303 | 
| Company DUNS | 653842898 | 
| Company Name | Guangdong Yuehua Medical Instrument Factory 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 | 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 | false | 
| OTC Over-The-Counter | false | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 06944749500305 [Primary] | 
| FNM | Mattress, Air Flotation, Alternating Pressure | 
| Steralize Prior To Use | false | 
| Device Is Sterile | false | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2023-07-07 | 
| Device Publish Date | 2023-06-29 | 
Mark Image Registration | Serial  | Company  Trademark Application Date  | 
|---|---|
![]() YHMED  79129791  4611703 Live/Registered  | 
        GUANGDONG YUEHUA MEDICAL INSTRUMENT FACTORY CO., LTD.  2013-04-02  |