Primary Device ID | 16944932759395 |
NIH Device Record Key | e85f51e8-04c6-4a24-8dbd-49782b1cb80f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Endobronchial Tube |
Version Model Number | A03A023910 |
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 | 06944932759398 [Primary] |
GS1 | 16944932759395 [Package] Contains: 06944932759398 Package: Box [1 Units] In Commercial Distribution |
GS1 | 26944932759392 [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 |