Primary Device ID | 00810136730050 |
NIH Device Record Key | 56ee7a55-f211-47c5-b494-95099779519b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GMP Medicare |
Version Model Number | L |
Company DUNS | 894495865 |
Company Name | GMP MEDICARE SDN. BHD. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | Labeling does not contain MRI Safety Information |
Human Cell/Tissue Product | false |
Device Kit | true |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | false |
OTC Over-The-Counter | false |