| Primary Device ID | 06970283489394 | 
| NIH Device Record Key | 1866f981-c544-493f-a722-f22dd06f599d | 
| Commercial Distribution Status | In Commercial Distribution | 
| Brand Name | UE Intubation Stylet | 
| Version Model Number | P3 | 
| Company DUNS | 542992969 | 
| Company Name | Zhejiang UE Medical Corp | 
| Device Count | 1 | 
| DM Exempt | false | 
| Pre-market Exempt | true | 
| 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 | 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 | 
| Phone | +8657687788798 | 
| export@ueworld.com | |
| Phone | +8657687788798 | 
| export@ueworld.com | |
| Phone | +8657687788798 | 
| export@ueworld.com | |
| Phone | +8657687788798 | 
| export@ueworld.com | |
| Phone | +8657687788798 | 
| export@ueworld.com | |
| Phone | +8657687788798 | 
| export@ueworld.com | |
| Phone | +8657687788798 | 
| export@ueworld.com | |
| Phone | +8657687788798 | 
| export@ueworld.com | |
| Phone | +8657687788798 | 
| export@ueworld.com | |
| Phone | +8657687788798 | 
| export@ueworld.com | |
| Phone | +8657687788798 | 
| export@ueworld.com | |
| Phone | +8657687788798 | 
| export@ueworld.com | |
| Phone | +8657687788798 | 
| export@ueworld.com | |
| Phone | +8657687788798 | 
| export@ueworld.com | |
| Phone | +8657687788798 | 
| export@ueworld.com | |
| Phone | +8657687788798 | 
| export@ueworld.com | |
| Phone | +8657687788798 | 
| export@ueworld.com | |
| Phone | +8657687788798 | 
| export@ueworld.com | 
| Device Issuing Agency | Device ID | 
|---|---|
| GS1 | 06970283489394 [Primary] | 
| BSR | Stylet, Tracheal Tube | 
| Steralize Prior To Use | false | 
| Device Is Sterile | true | 
| Public Version Status | New | 
| Device Record Status | Published | 
| Public Version Number | 1 | 
| Public Version Date | 2024-12-25 | 
| Device Publish Date | 2024-12-17 | 
| 06970283489424 | The device is intended to introduce devices into cavity or tissue. | 
| 06970283489394 | The device is intended to introduce devices into cavity or tissues. |