Primary Device ID | 16944932774862 |
NIH Device Record Key | 147a5153-4def-4e56-a65e-845195907c93 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Endotracheal Tube with Evacuation Lumen |
Version Model Number | A01F01751F |
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 | 06944932774865 [Primary] |
GS1 | 16944932774862 [Package] Contains: 06944932774865 Package: Box [10 Units] In Commercial Distribution |
GS1 | 26944932774869 [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 |
16944932784144 | PU Cuff 9.0 DEHP FREE |
16944932784120 | PU Cuff 8.5 DEHP FREE |
16944932784106 | PU Cuff 8.0 DEHP FREE |
16944932784083 | PU Cuff 7.5 DEHP FREE |
16944932784069 | PU Cuff 7.0 DEHP FREE |
16944932784045 | PU Cuff 6.5 DEHP FREE |
16944932784021 | PU Cuff 6.0 DEHP FREE |
16944932774923 | PVC DEHP Free Cuff 9.0 |
16944932774909 | PVC DEHP Free Cuff 8.5 |
16944932774886 | PVC DEHP Free Cuff 8.0 |
16944932774862 | PVC DEHP Free Cuff 7.5 |
16944932774848 | PVC DEHP Free Cuff 7.0 |
16944932774824 | PVC DEHP Free Cuff 6.5 |
16944932774800 | PVC DEHP Free Cuff 6.0 |