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Meyerding Retractor 7234-40

by Koros USA, Inc.

Meyerding Retractor 7234-40 is a Class I device made by Koros USA, Inc., listed in FDA GUDID since 1 Sep 2021 (UDI-DI 10840199508546), 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 Number10840199508546 UDI-DI Date1 Sep 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  • Withdrawn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
Meyerding Retractor
Generic name
Hand-held surgical retractor, reusable
Model / Ref / Catalog
7234-40
Primary DI / UDI-DI
10840199508546
FDA product code
GAD
GMDN term
Hand-held surgical retractor, reusable
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
Sterilisation method
Moist Heat or Steam Sterilization

Related devices

Category: Hand-held surgical retractor, reusable

Similar devices in this category

Other devices filed under Hand-held surgical retractor, reusable.

Other devices from Koros USA, Inc.

See all devices from Koros USA, Inc. →

Properties

  • Sterilise before use
  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Serial number
Other properties (10, all answered No)