Primary Device ID | B3808FCBS1001020 |
NIH Device Record Key | 25b4341d-dc28-4872-835a-e89d00869099 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LMI CAROTID SHUNT WITH SAFETY BALLOON CATHETER |
Version Model Number | 8FCBS100-10-2 |
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 | B3808FCBS1001020 [Primary] |
MJN | Catheter, Intravascular Occluding, Temporary |
Steralize Prior To Use | true |
Device Is Sterile | true |
[B3808FCBS1001020]
Ethylene Oxide
[B3808FCBS1001020]
Ethylene Oxide
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2016-09-19 |
B3809FCBS4004020 | 9FCBS400-40-2 |
B3809FCBS4004010 | 9FCBS400-40-1 |
B3809FCBS1001020 | 9FCBS100-10-2 |
B3809FCBS1001010 | 9FCBS100-10-1 |
B3808FCBS4004020 | 8FCBS400-40-2 |
B3808FCBS4004010 | 8FCBS400-40-1 |
B3808FCBS1001020 | 8FCBS100-10-2 |
B3808FCBS1001010 | 8FCBS100-10-1 |
B38012FCBS4004020 | 12FCBS400-40-2 |
B38012FCBS4004010 | 12FCBS400-40-1 |
B38012FCBS1001020 | 12FCBS100-10-2 |
B38012FCBS1001010 | 12FCBS100-10-1 |
B38011FCBS4004020 | 11FCBS400-40-2 |
B38011FCBS4004010 | 11FCBS400-40-1 |
B38011FCBS1001020 | 11FCBS100-10-2 |
B38011FCBS1001010 | 11FCBS100-10-1 |
B38010FCBS4004020 | 10FCBS400-40-2 |
B38010FCBS4004010 | 10FCBS400-40-1 |
B38010FCBS1001020 | 10FCBS100-10-2 |
B38010FCBS1001010 | 10FCBS100-10-1 |