Primary Device ID | B3808FOCC400 |
NIH Device Record Key | 5c9351f5-f9f1-44b1-ac64-363f10f5d5d5 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LMI OCCLUSION CATHETER |
Version Model Number | 8FOCC40 |
Company DUNS | 878198993 |
Company Name | LUCAS MEDICAL INC |
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 | true |
RX Perscription | true |
OTC Over-The-Counter | false |
Device Issuing Agency | Device ID |
---|---|
HIBCC | B3808FOCC400 [Primary] |
DXE | Catheter, Embolectomy |
Steralize Prior To Use | true |
Device Is Sterile | true |
[B3808FOCC400]
Ethylene Oxide
[B3808FOCC400]
Ethylene Oxide
[B3808FOCC400]
Ethylene Oxide
[B3808FOCC400]
Ethylene Oxide
[B3808FOCC400]
Ethylene Oxide
[B3808FOCC400]
Ethylene Oxide
[B3808FOCC400]
Ethylene Oxide
[B3808FOCC400]
Ethylene Oxide
[B3808FOCC400]
Ethylene Oxide
[B3808FOCC400]
Ethylene Oxide
[B3808FOCC400]
Ethylene Oxide
[B3808FOCC400]
Ethylene Oxide
[B3808FOCC400]
Ethylene Oxide
[B3808FOCC400]
Ethylene Oxide
[B3808FOCC400]
Ethylene Oxide
[B3808FOCC400]
Ethylene Oxide
[B3808FOCC400]
Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 4 |
Public Version Date | 2019-03-21 |
Device Publish Date | 2016-09-02 |
B3808FOCC400 | 8FOCC40 |
B3808FOCC230 | 8FOCC23 |
B3807FOCC400 | 7FOCC40 |
B3807FOCC230 | 7FOCC23 |
B3806FOCC400 | 6FOCC40 |
B3806FOCC230 | 6FOCC23 |
B3805FOCC400 | 5FOCC40 |
B3805FOCC230 | 5FOCC23 |
B3804FOCC400 | 4FOCC40 |
B3804FOCC230 | 4FOCC23 |
B3803FOCC400 | 3FOCC40 |
B3803FOCC230 | 3FOCC23 |