| Primary Device ID | 16944932759401 |
| NIH Device Record Key | 991d859b-587c-43b9-8b32-34769bd92d5e |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Endobronchial Tube |
| Version Model Number | A03A024110 |
| Company DUNS | 544811862 |
| Company Name | Well Lead Medical 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 | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | true |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 06944932759404 [Primary] |
| GS1 | 16944932759401 [Package] Contains: 06944932759404 Package: Box [1 Units] In Commercial Distribution |
| GS1 | 26944932759408 [Package] Package: Carton [20 Units] In Commercial Distribution |
| CBI | Tube, Tracheal/Bronchial, Differential Ventilation (W/Wo Connector) |
| Steralize Prior To Use | false |
| Device Is Sterile | true |
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2023-12-04 |
| Device Publish Date | 2023-11-24 |
| 16944932759401 | right Fr41 |
| 16944932759395 | right Fr39 |
| 16944932759388 | right Fr37 |
| 16944932759371 | right Fr35 |
| 16944932759364 | right Fr32 |
| 16944932759357 | right Fr28 |
| 16944932759173 | left Fr41 |
| 16944932759166 | left Fr39 |
| 16944932759159 | left Fr37 |
| 16944932759142 | left Fr35 |
| 16944932759135 | left Fr32 |
| 16944932759128 | left Fr28 |