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Cyber Blade CVA000002

by Quanta System SpA

Cyber Blade CVA000002 is a Class II device made by Quanta System SpA, listed in FDA GUDID since 4 Feb 2021 (UDI-DI 08059173391707), 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 Number08059173391707 UDI-DI Date4 Feb 2021ListedStatusListed 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  • Withdrawn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
Cyber Blade
Generic name
Tissue morcellation system handpiece, battery-powered
Model / reference
CVA000002
Primary DI / UDI-DI
08059173391707
FDA product code
GCJ
GMDN term
Tissue morcellation system handpiece, battery-powered
Device class
Class II
Regulation number
876.1500
GUDID distribution status
In Commercial Distribution

Similar devices

Other devices filed under FDA product code GCJ (Laparoscope, General & Plastic Surgery).

Other devices from Quanta System SpA

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Properties

  • Supplied sterile
  • Single use
  • Prescription use
  • Serial number
  • Expiration date
Other properties (10, all answered No)