Primary Device ID | 00664816002308 |
NIH Device Record Key | 60669100-f5ff-4ddd-ad9b-4dd6877fc6e3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | LW Scientific, Inc` |
Version Model Number | ICL-010L-D032 |
Catalog Number | ICL-010L-D032 |
Company DUNS | 785335381 |
Company Name | LW SCIENTIFIC, INC. |
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 | true |
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 |