Skip to content

Flex 25778

by Medrobotics Corporation

Flex 25778 is a Class II device made by Medrobotics Corporation, listed in FDA GUDID since 1 Apr 2019 (UDI-DI 00850190004766), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00850190004766 UDI-DI Date1 Apr 2019ListedStatusListed 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  • Withdrawn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
Flex
Generic name
Robotic surgical telemanipulation system
Model / reference
25778
Primary DI / UDI-DI
00850190004766
FDA product code
EOB
GMDN term
Robotic surgical telemanipulation system
Device class
Class II
Regulation number
874.4760
GUDID distribution status
In Commercial Distribution

Related devices

Category: Robotic surgical arm system

Similar devices in this category

Other devices filed under Robotic surgical arm system.

Other devices from Medrobotics Corporation

  • Flex 25386

    Class II

  • Flex 24324-L

    Class II

  • Flex 50124PKG

    Class I

  • Flex 50208PKG

    Class I

See all devices from Medrobotics Corporation →

Properties

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