Symphion Spare Footswitch FG-0656

GUDID 00850033976113

Symphion Operative Hysteroscopy System Spare Footswitch only for use with Symphion Controller

Minerva Surgical, Inc.

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Primary Device ID00850033976113
NIH Device Record Keyc972409e-0c84-4e4d-a919-6816f22a6147
Commercial Distribution StatusIn Commercial Distribution
Brand NameSymphion Spare Footswitch
Version Model NumberFG-0656
Catalog NumberFG-0656
Company DUNS829616478
Company NameMinerva Surgical, Inc.
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone855-646-7874
Emailcustomerservice@minervasurgical.com
Phone855-646-7874
Emailcustomerservice@minervasurgical.com
Phone855-646-7874
Emailcustomerservice@minervasurgical.com
Phone855-646-7874
Emailcustomerservice@minervasurgical.com
Phone855-646-7874
Emailcustomerservice@minervasurgical.com
Phone855-646-7874
Emailcustomerservice@minervasurgical.com
Phone855-646-7874
Emailcustomerservice@minervasurgical.com
Phone855-646-7874
Emailcustomerservice@minervasurgical.com
Phone855-646-7874
Emailcustomerservice@minervasurgical.com
Phone855-646-7874
Emailcustomerservice@minervasurgical.com
Phone855-646-7874
Emailcustomerservice@minervasurgical.com
Phone855-646-7874
Emailcustomerservice@minervasurgical.com
Phone855-646-7874
Emailcustomerservice@minervasurgical.com
Phone855-646-7874
Emailcustomerservice@minervasurgical.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100850033976113 [Primary]
GS108714729893318 [Previous]

FDA Product Code

PGTInsufflator, Hysteroscopic, Fluid, Closed-Loop Recirculation With Cutter-Coagulator, Endoscopic, Bipolar

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-05-11
Device Publish Date2022-05-03

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