Primary Device ID | 04547410347517 |
NIH Device Record Key | 96db15c9-2ea9-47d3-9cc6-b15da5c5a46c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Needle guide 12G (C-L,C-S) |
Version Model Number | NEEDLE GUIDE C 12G E |
Company DUNS | 713565195 |
Company Name | FUJIFILM CORPORATION |
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 | 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 | false |
OTC Over-The-Counter | false |
Phone | +018002728465 |
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Phone | +018002728465 |
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Phone | +018002728465 |
xxx@xxx.xxx |
Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
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Device Size Text, specify | 0 |
Device Size Text, specify | 0 |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04547410347517 [Primary] |
MUE | Full field digital,system,x-ray,mammographic |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2017-02-03 |
04547410515893 - FUJIFILM | 2024-10-14 This product is intended to be used in combination with the compatible endoscopes, camera head, light source and light guide to |
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