← Back to catalogue

Emprint

FDA UDI

Class II (US FDA UDI)

by Covidien LP

Identity

Trade Name
Emprint FDA UDI
Generic Name
Radiation therapy software FDA UDI
Device Name
Emprint Ablation Visualization Application V2.0 FDA UDI
Model / Reference
CAVA FDA UDI
Description
Emprint Ablation Visualization Application V2.0 FDA UDI

Identifiers

Primary DI / UDI-DI
10884521783928 FDA UDI
510(k) Number
K180192 FDA UDI
FDA Product Code
LLZ FDA UDI
GMDN Term
Radiation therapy software FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
892.2050 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

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

No

FDA UDI

Category: Radiation therapy software

Emprint by Covidien LP — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Radiation therapy software.

Cleared under the same submission

K180192 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
Covidien LP

Sources (1)

  • FDA UDI b7669a67-e518-4d5a-830d-c5e72c555e62 35 fields · synced May 30, 2026