Primary Device ID | 00852728008857 |
NIH Device Record Key | b620aee8-4f8c-4e28-b471-a879c6d4ac21 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | SEILER MEDICAL DIVIVSION |
Version Model Number | 3DV-500 |
Company DUNS | 006265334 |
Company Name | SEILER INSTRUMENT AND MANUFACTURING COMPANY, INCORPORATED |
Device Count | 1 |
DM Exempt | true |
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 | false |
Serial Number | true |
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 |
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