Primary Device ID | 00860011763208 |
NIH Device Record Key | 7c70f1fe-7fa2-46f3-afc3-5e9402b4cc68 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | NDDR and CDCS |
Version Model Number | 2.3 |
Company DUNS | 102958199 |
Company Name | CIELOWORKS, 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 | true |
Device Kit | false |
Device Combination Product | false |
Single Use | false |
Lot Batch | false |
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 | true |
OTC Over-The-Counter | false |