Primary Device ID | 04058749063943 |
NIH Device Record Key | 63995e59-1411-4fcb-ae18-170ce57ca886 |
Commercial Distribution Status | In Commercial Distribution |
Version Model Number | NNU-0X |
Catalog Number | NNU-0X |
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 | 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 | true |
OTC Over-The-Counter | false |
Phone | 800 334-5464 |
info@fehlingsurgical.com |
Device Issuing Agency | Device ID |
---|---|
GS1 | 04058749063943 [Primary] |
HAE | Rongeur, Manual |
Steralize Prior To Use | true |
Device Is Sterile | false |
[04058749063943]
Moist Heat or Steam Sterilization
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2019-07-17 |
Device Publish Date | 2018-09-17 |
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