Primary Device ID | 00841732143098 |
NIH Device Record Key | e4a5e0a0-8799-4308-ae79-51f78763957f |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | GENERIC |
Version Model Number | 100.7590 |
Company DUNS | 080138504 |
Company Name | CTL Medical Corporation |
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 | 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 |
Phone | 214-545-5820 |
schedule@ctlamedica.com | |
Phone | 214-545-5820 |
schedule@ctlamedica.com | |
Phone | 214-545-5820 |
schedule@ctlamedica.com | |
Phone | 214-545-5820 |
schedule@ctlamedica.com | |
Phone | 214-545-5820 |
schedule@ctlamedica.com | |
Phone | 214-545-5820 |
schedule@ctlamedica.com | |
Phone | 214-545-5820 |
schedule@ctlamedica.com | |
Phone | 214-545-5820 |
schedule@ctlamedica.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00841732143098 [Primary] |
HXX | Screwdriver |
Steralize Prior To Use | true |
Device Is Sterile | false |
[00841732143098]
Moist Heat or Steam Sterilization
[00841732143098]
Moist Heat or Steam Sterilization
[00841732143098]
Moist Heat or Steam Sterilization
[00841732143098]
Moist Heat or Steam Sterilization
[00841732143098]
Moist Heat or Steam Sterilization
[00841732143098]
Moist Heat or Steam Sterilization
[00841732143098]
Moist Heat or Steam Sterilization
[00841732143098]
Moist Heat or Steam Sterilization
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2025-06-12 |
Device Publish Date | 2025-06-04 |