Primary Device ID | 04058749000092 |
NIH Device Record Key | 8d116a63-c709-46b1-897b-800cc63a18a2 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | MOA-9 |
Catalog Number | MOA-9 |
Company DUNS | 315028238 |
Company Name | Fehling Instruments GmbH & Co. KG |
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 | true |
Lot Batch | true |
Serial Number | false |
Manufacturing Date | false |
Expiration Date | true |
Donation Id Number | false |
Contains Natural Rubber Latex | false |
Labeled No Natural Rubber Latex | false |
RX Perscription | true |
OTC Over-The-Counter | false |
Phone | 800 334-5464 |
info@fehlingsurgical.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04058749000092 [Primary] |
DWZ | Device, Biopsy, Endomyocardial |
Steralize Prior To Use | false |
Device Is Sterile | true |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 3 |
Public Version Date | 2018-07-06 |
Device Publish Date | 2017-06-23 |
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