| Primary Device ID | 00810136730043 |
| NIH Device Record Key | 1f95fa56-0b23-4733-890c-dc93f66de99d |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | GMP Medicare |
| Version Model Number | M |
| 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 | true |
| 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 |