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 |