Primary Device ID | 04547410217995 |
NIH Device Record Key | 93750483-99a9-44a7-993a-698b22ddc5aa |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Needle guide cover 10 |
Version Model Number | NEEDLE GUIDE COVER 10 E |
Company DUNS | 713565195 |
Company Name | FUJIFILM CORPORATION |
Device Count | 10 |
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 |
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Phone | +018002728465 |
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Phone | +018002728465 |
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Phone | +018002728465 |
xxx@xxx.xxx |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04547410217995 [Primary] |
GS1 | 84547410217991 [Unit of Use] |
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 | 2016-09-16 |
14547410477150 - FUJIFILM | 2025-06-09 This product is intended for the visualization of the upper digestive tract, specifically for the observation, diagnosis, and en |
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04573596213216 - UST-9104-5 | 2025-03-28 Probe |