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Mima-Pro

FDA UDI

Class II (US FDA UDI)

by Mima-Pro (Nan Tong) Scientific Inc.

Identity

Trade Name
Mima-Pro FDA UDI
Generic Name
Microwave ablation system probe, non-powered FDA UDI
Device Name
WATER-COOLED MICROWAVE ABLATION APPLICATOR FDA UDI
Model / Reference
MP18200T16 FDA UDI
Description
WATER-COOLED MICROWAVE ABLATION APPLICATOR FDA UDI

Identifiers

Primary DI / UDI-DI
26973913880107 FDA UDI
FDA Product Code
NEY FDA UDI
GMDN Term
Microwave ablation system probe, non-powered 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

Yes

FDA UDI
Sterilization Method
Ethylene Oxide FDA UDI

Category: Microwave ablation system probe, non-powered

Mima-Pro by Mima-Pro (Nan Tong) Scientific Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Microwave ablation system probe, non-powered.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Mima-Pro (Nan Tong) Scientific Inc.

Sources (1)

  • FDA UDI 4c5b20cb-8a83-4b00-b02c-a56f80cb2162 33 fields · synced May 30, 2026