MOA-1

GUDID 04058749000016

Biopsy forceps, single use sterile, 1,6 x 510 mm

Fehling Instruments GmbH & Co. KG

Endomyocardial biopsy forceps, single-use
Primary Device ID04058749000016
NIH Device Record Keyed3aa584-8759-477b-b285-b74d80b7c752
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberMOA-1
Catalog NumberMOA-1
Company DUNS315028238
Company NameFehling Instruments GmbH & Co. KG
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone800 334-5464
Emailinfo@fehlingsurgical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS104058749000016 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

DWZDevice, Biopsy, Endomyocardial

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2017-06-23

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