Plasma IQ Electrode Straight (1 piece) 200-1201

GUDID 00850017374010

1 straight electrode for use with Plasma IQ

NEAUVIA NORTH AMERICA, INC.

Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use Electrosurgical handpiece, single-use
Primary Device ID00850017374010
NIH Device Record Keybc3bfb09-277c-4dbb-96b5-11b06f2df216
Commercial Distribution StatusIn Commercial Distribution
Brand NamePlasma IQ Electrode Straight (1 piece)
Version Model NumberAEP-101
Catalog Number200-1201
Company DUNS117030786
Company NameNEAUVIA NORTH AMERICA, 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 Usetrue
Lot Batchtrue
Serial Numbertrue
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numbertrue
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone984-777-5292
Emailmisty@neauvia-us.com
Phone984-777-5292
Emailmisty@neauvia-us.com
Phone984-777-5292
Emailmisty@neauvia-us.com
Phone984-777-5292
Emailmisty@neauvia-us.com
Phone984-777-5292
Emailmisty@neauvia-us.com
Phone984-777-5292
Emailmisty@neauvia-us.com
Phone984-777-5292
Emailmisty@neauvia-us.com
Phone984-777-5292
Emailmisty@neauvia-us.com
Phone984-777-5292
Emailmisty@neauvia-us.com
Phone984-777-5292
Emailmisty@neauvia-us.com
Phone984-777-5292
Emailmisty@neauvia-us.com
Phone984-777-5292
Emailmisty@neauvia-us.com
Phone984-777-5292
Emailmisty@neauvia-us.com
Phone984-777-5292
Emailmisty@neauvia-us.com
Phone984-777-5296
Emailjoy@neauvia-us.com
Phone984-777-5296
Emailjoy@neauvia-us.com
Phone984-777-5296
Emailjoy@neauvia-us.com
Phone984-777-5296
Emailjoy@neauvia-us.com
Phone984-777-5296
Emailjoy@neauvia-us.com
Phone984-777-5296
Emailjoy@neauvia-us.com
Phone984-777-5296
Emailjoy@neauvia-us.com
Phone984-777-5296
Emailjoy@neauvia-us.com
Phone984-777-5296
Emailjoy@neauvia-us.com
Phone984-777-5296
Emailjoy@neauvia-us.com
Phone984-777-5296
Emailjoy@neauvia-us.com
Phone984-777-5296
Emailjoy@neauvia-us.com
Phone984-777-5296
Emailjoy@neauvia-us.com
Phone984-777-5296
Emailjoy@neauvia-us.com
Phone984-777-5296
Emailjoy@neauvia-us.com
Phone984-777-5296
Emailjoy@neauvia-us.com
Phone984-777-5296
Emailjoy@neauvia-us.com
Phone984-777-5296
Emailjoy@neauvia-us.com
Phone984-777-5296
Emailjoy@neauvia-us.com
Phone984-777-5296
Emailjoy@neauvia-us.com
Phone984-777-5296
Emailjoy@neauvia-us.com
Phone984-777-5296
Emailjoy@neauvia-us.com
Phone984-777-5296
Emailjoy@neauvia-us.com
Phone984-777-5296
Emailjoy@neauvia-us.com
Phone984-777-5296
Emailjoy@neauvia-us.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100850017374010 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

GEIElectrosurgical, Cutting & Coagulation & Accessories

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-09-22
Device Publish Date2020-09-14

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