Primary Device ID | 10351688518217 |
NIH Device Record Key | 5ea7fe4b-d02e-49c1-a8b9-baae3515bdf2 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Smiths Medical |
Version Model Number | 358025 |
Company DUNS | 118112924 |
Company Name | SMITHS MEDICAL ASD, INC. |
Device Count | 1 |
DM Exempt | false |
Pre-market Exempt | false |
MRI Safety Status | MR Conditional |
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 | 10351688518217 [Primary] |
JOH | Tube tracheostomy and tube cuff |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 5 |
Public Version Date | 2024-09-12 |
Device Publish Date | 2015-07-29 |
10351688518248 | 358040 |
10351688518231 | 358035 |
10351688518224 | 358030 |
10351688518217 | 358025 |
10351688518200 | 353055 |
10351688518194 | 353050 |
10351688518187 | 353045 |
10351688518170 | 353040 |
10351688518163 | 353035 |
10351688518156 | 353030 |
10351688518149 | 353025 |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
SMITHS MEDICAL 85881138 4800141 Live/Registered |
Smiths Medical ASD, Inc. 2013-03-20 |