← Back to catalogue

Neogen

FDA UDI

Class II (US FDA UDI)

by Energist, Ltd.

Identity

Trade Name
Neogen FDA UDI
Generic Name
Nitrogen plasma skin surface treatment system FDA UDI
Device Name
Neogen Trolley Complete Gry FDA UDI
Model / Reference
Trolley Gry FDA UDI
Description
Neogen Trolley Complete Gry FDA UDI

Identifiers

Catalog Number
930-020 FDA UDI
Primary DI / UDI-DI
05060440520280 FDA UDI
510(k) Number
K132754 FDA UDI
FDA Product Code
GEI FDA UDI
GMDN Term
Nitrogen plasma skin surface treatment system 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

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Nitrogen plasma skin surface treatment system

Neogen by Energist, Ltd. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Nitrogen plasma skin surface treatment system.

Cleared under the same submission

K132754 also covers:

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

Is this your device? Claim it to add documentation and request validation.

Manufacturer

Manufacturer
Energist, Ltd.

Sources (1)

  • FDA UDI 6f012e2c-44e2-44d3-bec9-e70fe7c498a8 35 fields · synced Jun 8, 2026