Primary Device ID | 00846159028843 |
NIH Device Record Key | 5a6b8859-6ae5-41a3-8fc7-6b6c89cff3f7 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SCANLAN Minimally-Invasive Instrumentation |
Version Model Number | 9909-914 |
Catalog Number | 9909-914 |
Company DUNS | 023055619 |
Company Name | SCANLAN INTERNATIONAL 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 | 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 | true |
OTC Over-The-Counter | false |
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