| 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 |