Primary Device ID | 30817357021838 |
NIH Device Record Key | ac7d5d35-2d9f-46f7-9e7e-e552521b06ef |
Commercial Distribution Discontinuation | 2019-07-31 |
Commercial Distribution Status | Not in Commercial Distribution |
Brand Name | CTC |
Version Model Number | VP501L |
Company DUNS | 177939027 |
Company Name | HYGIA HEALTH SERVICES, 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 | false |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | false |
OTC Over-The-Counter | false |