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Flex 50124PKG

by Medrobotics Corporation

Flex 50124PKG is a Class I device made by Medrobotics Corporation, listed in FDA GUDID since 9 Apr 2019 (UDI-DI 00850190004315), 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 Number00850190004315 UDI-DI Date9 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  • Withdrawn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 retractor
Model / reference
50124PKG
Primary DI / UDI-DI
00850190004315
FDA product code
KAL
GMDN term
Robotic surgical retractor
Device class
Class I
Regulation number
874.4420
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Robotic surgical retractor

Similar devices

Other devices filed under FDA product code KAL (Retractor, Ent).

Other devices from Medrobotics Corporation

  • Flex 25386

    Class II

  • Flex 24324-L

    Class II

  • Flex 50208PKG

    Class I

  • Flex 25776

    Class II

See all devices from Medrobotics Corporation →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)