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Emprint CAGEN1ZD

by Covidien LP

Emprint CAGEN1ZD is a microwave hyperthermia system (FDA Class II) made by Covidien LP, listed in FDA GUDID since 24 Sep 2016 (UDI-DI 10884521552579), registry data as of 23 Oct 2026.

Listed FDA GUDID listing, no authorization on record

Valid until

Not applicable

Database listing, no authorization

FDA recalls

Not checked

No FDA submission to match recalls against

Documents

None

No authorization documents

Trust

Unverified

Source GUDID, synced 23 Oct 2026.

Regulatory status

as of registry sync 23 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number10884521552579 UDI-DI Date24 Sep 2016ListedStatusListed GUDID: in commercial distribution

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — GUDID listing Listed

Specification

GUDID

Trade name
Emprint
Generic name
Microwave hyperthermia system
Model / reference
CAGEN1ZD
Primary DI / UDI-DI
10884521552579
FDA product code
NEY, GEI
GMDN term
Microwave hyperthermia system
Device class
Class II
Regulation number
878.4400
GUDID distribution status
In Commercial Distribution

Related devices

Category: Microwave hyperthermia system

Similar devices in this category

Other devices filed under Microwave hyperthermia system.

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See all devices from Covidien LP →

Properties

  • Prescription use
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)