Primary Device ID | 00843356101812 |
NIH Device Record Key | a39d5941-4ad0-47f5-9ef0-bcd6f8acc47e |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Use Assigned GITN before 12/31/2024. Currently unpublished. Will publish on 12 |
Version Model Number | GIC190R |
Company DUNS | 103169095 |
Company Name | CYGNUS MEDICAL L.L.C. |
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 | true |
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 |