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Blueendo 55-000051

by TROKAMED GmbH

Blueendo 55-000051 is a Class II device made by TROKAMED GmbH, listed in FDA GUDID since 27 Feb 2026 (UDI-DI 04251303824961), 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 Number04251303824961 UDI-DI Date27 Feb 2026ListedStatusListed 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  • Withdrawn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
Blueendo
Generic name
Tissue morcellation system
Model / Ref / Catalog
55-000051
Primary DI / UDI-DI
04251303824961
FDA product code
HET
GMDN term
Tissue morcellation system
Device class
Class II
Regulation number
884.1720
GUDID distribution status
In Commercial Distribution

Other devices from TROKAMED GmbH

See all devices from TROKAMED GmbH →

Properties

  • Prescription use
  • Lot / batch number
  • Manufacturing date
Other properties (12, all answered No)