Primary Device ID | B839T2YW19J3Y4B03F5980 |
NIH Device Record Key | 3104173f-c6c0-4777-a037-ff53d349304c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | CascoCup |
Version Model Number | 5YHAR288BT2YW19J3Y4B03F598 |
Company DUNS | 604286695 |
Company Name | CASCO BAY MOLDING LTD. |
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 |