| Primary Device ID | 16944932729640 | 
| NIH Device Record Key | 547d1748-c024-43b5-81a2-a270808946e7 | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | Well Lead Endotracheal Tube with Evacuation Lumen | 
| Version Model Number | A01F017510 | 
| 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 | 06944932729643 [Primary] | 
| GS1 | 16944932729640 [Package] Contains: 06944932729643 Package: Box [10 Units] In Commercial Distribution  | 
| GS1 | 26944932729647 [Package] Package: Carton [10 Units] In Commercial Distribution  | 
| BTR | Tube, Tracheal (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 | 2024-02-05 | 
| Device Publish Date | 2024-01-27 | 
| 16944932737003 | PVC Cuff 9.0 | 
| 16944932730448 | PVC Cuff 6.5 | 
| 16944932730431 | PVC Cuff 6.0 | 
| 16944932729664 | PVC Cuff 8.5 | 
| 16944932729657 | PVC Cuff 8.0 | 
| 16944932729640 | PVC Cuff 7.5 | 
| 16944932729633 | PVC Cuff 7.0 |