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Plasma IQ Handpiece

FDA UDI

Class II (US FDA UDI)

by Neauvia North America, Inc

Identity

Trade Name
Plasma IQ Handpiece FDA UDI
Generic Name
Electrosurgical handpiece, single-use FDA UDI
Device Name
Individual handpiece for the Plasma IQ System FDA UDI
Model / Reference
PLA-752 FDA UDI
Description
Individual handpiece for the Plasma IQ System FDA UDI

Identifiers

Catalog Number
300-1202 FDA UDI
Primary DI / UDI-DI
00850017374041 FDA UDI
510(k) Number
K192813 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Electrosurgical handpiece, single-use FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrosurgical handpiece, single-use

Plasma IQ Handpiece by Neauvia North America, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical handpiece, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI ca78c130-aa8d-416d-9e85-3f67414c4fe7 36 fields · synced May 30, 2026