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Fraxis Duo 25Pin Needle Tip

FDA UDI

Class II (US FDA UDI)

by Ilooda.co., Ltd

Identity

Trade Name
Fraxis Duo 25Pin Needle Tip FDA UDI
Generic Name
Electrosurgical handpiece/electrode holder, single-use FDA UDI
Device Name
MTR-AC-25 FDA UDI
Model / Reference
MTR-AC-25 FDA UDI
Description
MTR-AC-25 FDA UDI

Identifiers

Primary DI / UDI-DI
08800023200058 FDA UDI
510(k) Number
K160312 FDA UDI
FDA Product Code
GEI FDA UDI
OUH FDA UDI
GMDN Term
Electrosurgical handpiece/electrode holder, 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

Yes

FDA UDI

Single Use

Yes

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

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Electrosurgical handpiece/electrode holder, single-use

Fraxis Duo 25Pin Needle Tip by Ilooda.co., Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Electrosurgical handpiece/electrode holder, single-use.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Ilooda.co., Ltd

Sources (1)

  • FDA UDI 64e63122-d9ec-429c-87af-c302b63767f5 35 fields · synced May 30, 2026