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Emprint CAGEN1

by Covidien LP

Emprint CAGEN1 is a microwave ablation system generator (FDA Class II) made by Covidien LP, listed in FDA GUDID since 15 Aug 2017 (UDI-DI 10884521190771), 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 Number10884521190771 UDI-DI Date15 Aug 2017ListedStatusListed 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  • Withdrawn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 ablation system generator
Model / reference
CAGEN1
Primary DI / UDI-DI
10884521190771
FDA product code
NEY, GEI
GMDN term
Microwave ablation system generator
Device class
Class II
Regulation number
878.4400
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code NEY (SYSTEM, ABLATION, MICROWAVE AND ACCESSORIES).

Other devices from Covidien LP

  • LigaSure MRASILF19

    Class II
  • Shiley 110860

    Class II
  • Shiley 110865

    Class II
  • Shiley 110870

    Class II

See all devices from Covidien LP →

Properties

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