| Primary Device ID | 08800017901930 |
| NIH Device Record Key | 5818fa63-0a24-4626-83fc-4d49c096ac31 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | C-Warmer |
| Version Model Number | Dual |
| Company DUNS | 688797315 |
| Company Name | DXM CO., LTD |
| 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 | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | false |
| Serial Number | true |
| 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 | 08800017901930 [Primary] |
| EFC | Warmer, Anesthetic Tube |
| Steralize Prior To Use | false |
| Device Is Sterile | false |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-07-23 |
| Device Publish Date | 2024-07-15 |
| 08800017900117 | C-Warmer is designed to enhance both the doctor' and the patiends'. A themostatically-controlled |
| 08800017900100 | C-Warmer is designed to enhance both the doctor' and the patiends'. A themostatically-controlled |
| 08800017900094 | C-Warmer is designed to enhance both the doctor' and the patiends'. A themostatically-controlled |
| 08800017900087 | C-Warmer is designed to enhance both the doctor' and the patiends'. A themostatically-controlled |
| 08800017901930 | C-Warmer is designed to enhance both the doctor' and the patiends'. A themostatically-controlled |