Primary Device ID | 00840117317611 |
NIH Device Record Key | 336d681d-e7e3-49ad-9f4b-6f7c51e8af67 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Resp-O2 Endotracheal Tube With Stylette, Cuffed, 6.5 mm |
Version Model Number | 36250 |
Company DUNS | 008124539 |
Company Name | DYNAREX CORPORATION |
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 | false |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00840117313224 [Package] Package: Box [10 Units] In Commercial Distribution |
GS1 | 00840117313231 [Package] Contains: 00840117313224 Package: Case [10 Units] In Commercial Distribution |
GS1 | 00840117317611 [Primary] |
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 | 2022-05-23 |
Device Publish Date | 2022-05-15 |