| Primary Device ID | 16970462546440 |
| NIH Device Record Key | e0780612-3416-4234-9dc2-491739546555 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Single-Use Rhinolaryngoscope |
| Version Model Number | RH-M40H |
| Company DUNS | 403655303 |
| Company Name | Shenzhen HugeMed Medical Technical Development 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 | true |
| Lot Batch | false |
| Serial Number | true |
| Manufacturing Date | true |
| Expiration Date | true |
| 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 | 06970462546443 [Primary] |
| GS1 | 16970462546440 [Package] Contains: 06970462546443 Package: CASE [10 Units] Discontinued: 2024-06-11 Not in Commercial Distribution |
| GS1 | 26970462546447 [Package] Contains: 06970462546443 Package: CASE [5 Units] Discontinued: 2024-06-11 Not in Commercial Distribution |
| EOB | Nasopharyngoscope (Flexible Or Rigid) |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2024-06-19 |
| Device Publish Date | 2024-06-11 |
| 16970462546488 | RH-M32A |
| 16970462546440 | RH-M40H |
| 16970462546433 | RH-M52H |
| 16970462546426 | RH-M58H |
| 16970462546419 | RH-M22 |
| 16970462546402 | RH-M32 |
| 16970462546396 | RH-M40 |
| 16970462546389 | RH-M50 |
| 16970462546372 | RH-M52 |
| 16970462546365 | RH-M58 |