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Emprint

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name
Emprint FDA UDI
Generic Name
Microwave ablation system probe, non-powered FDA UDI
Device Name
Standard Percutaneous Antenna with Thermosphere Technology Large Spherical Ablation Zone FDA UDI
Model / Reference
CA20L1 FDA UDI
Description
Standard Percutaneous Antenna with Thermosphere Technology Large Spherical Ablation Zone FDA UDI

Identifiers

Primary DI / UDI-DI
10884521189546 FDA UDI
FDA Product Code
NEY FDA UDI
GEI 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

No

FDA UDI

Dimensions & Sizes

Size
Length — 20 Centimeter FDA UDI

Category: Microwave ablation system probe, non-powered

Emprint by Covidien LP — 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
Covidien LP

Sources (1)

  • FDA UDI a0789848-afc8-4077-887e-1fc1ac2582a2 36 fields · synced Jun 8, 2026