Primary Device ID | 00860010482681 |
NIH Device Record Key | bc9fdc34-113d-43a7-8338-86f8f6fa5b74 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | AcanthusTM |
Version Model Number | NCH |
Catalog Number | NCH |
Company DUNS | 065124205 |
Company Name | Acanthus Medical Creations LLC |
Device Count | 100 |
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 | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | true |
RX Perscription | true |
OTC Over-The-Counter | true |