Primary Device ID | 00858298006637 |
NIH Device Record Key | 1b50df4e-fcf4-4132-8a5b-8bae70eb659b |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Willow Go Flange Accessory Kit, 21 mm |
Version Model Number | LF2167 |
Company DUNS | 050917861 |
Company Name | EXPLORAMED NC7, 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 | false |
OTC Over-The-Counter | true |
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00858298006637 - Willow Go Flange Accessory Kit, 21 mm | 2022-09-08 Willow Go Flange Accessory Kit, 21 mm |