← Back to catalogue

Fraxis Duo Needle Handpiece

FDA UDI

Class II (US FDA UDI)

by CLASSYS Inc.

Identity

Trade Name
Fraxis Duo Needle Handpiece FDA UDI
Generic Name
Intradermal radio-frequency ablation system FDA UDI
Model / Reference
FRX-C2 FDA UDI

Identifiers

Primary DI / UDI-DI
08800016903669 FDA UDI
510(k) Number
K160312 FDA UDI
FDA Product Code
GEI FDA UDI
GEX FDA UDI
OUH FDA UDI
GMDN Term
Intradermal radio-frequency ablation system FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
878.4400 FDA UDI
878.4810 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

No

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

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Intradermal radio-frequency ablation system

Fraxis Duo Needle Handpiece by CLASSYS Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Intradermal radio-frequency ablation system.

Cleared under the same submission

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
CLASSYS Inc.

Sources (1)

  • FDA UDI d3ae4558-5f75-481d-b7a8-8df171922af7 33 fields · synced May 30, 2026