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Orchestra Plus

by Microport Crm SRL

Orchestra Plus is a Class III device made by Microport Crm SRL, listed in FDA GUDID since 5 Sep 2014 (UDI-DI 08031527013367), 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 Number08031527013367 UDI-DI Date5 Sep 2014ListedStatusListed 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  • Withdrawn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
Orchestra
Generic name
Cardiac pulse generator programmer
Model / reference
Plus
Primary DI / UDI-DI
08031527013367
FDA product code
NVZ
GMDN term
Cardiac pulse generator programmer
Device class
Class III
GUDID distribution status
In Commercial Distribution

Related devices

Category: Cardiac pulse generator programmer

Similar devices in this category

Other devices filed under Cardiac pulse generator programmer.

Other devices from Microport Crm SRL

See all devices from Microport Crm SRL →

Properties

  • Prescription use
  • Serial number
Other properties (13, all answered No)