← Back to catalogue

Epimed

FDA UDI

Class II (US FDA UDI)

by Minta Medical Limited

Identity

Trade Name
Epimed FDA UDI
Generic Name
Percutaneous radio-frequency ablation probe, denervation, monopolar, reusable FDA UDI
Device Name
R-F™ Probe Assembly Minta, 5cm (Stainless Steel) FDA UDI
Model / Reference
297-5 FDA UDI
Description
R-F™ Probe Assembly Minta, 5cm (Stainless Steel) FDA UDI

Identifiers

Catalog Number
297-5 FDA UDI
Primary DI / UDI-DI
05060224333051 FDA UDI
510(k) Number
K090608 FDA UDI
FDA Product Code
GXI FDA UDI
GMDN Term
Percutaneous radio-frequency ablation probe, denervation, monopolar, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
882.4725 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
MRI Safety
MR Unsafe FDA UDI

Dimensions & Sizes

Size
Length — 5 Centimeter FDA UDI

Category: Percutaneous radio-frequency ablation probe, denervation, monopolar, reusable

Epimed by Minta Medical Limited — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Percutaneous radio-frequency ablation probe, denervation, monopolar, reusable.

Cleared under the same submission

K090608 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
Minta Medical Limited

Sources (1)

  • FDA UDI 1f2e23ce-2f30-4e62-b174-572671d7a2e7 38 fields · synced May 30, 2026