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Medline MEDKB12SS

by Medline Industries, Inc.

Medline MEDKB12SS is a Class I device made by Medline Industries, Inc., listed in FDA GUDID since 2 Jun 2025 (UDI-DI 10197344138968), 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 Number10197344138968 UDI-DI Date2 Jun 2025ListedStatusListed 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  • Withdrawn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
Medline
Generic name
Kick bucket
Model / Ref / Catalog
MEDKB12SS
Primary DI / UDI-DI
10197344138968
FDA product code
FSM
GMDN term
Kick bucket
Device class
Class I
Regulation number
878.4800
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Related devices

Category: Kick bucket

Similar devices

Other devices filed under FDA product code FSM (TRAY, SURGICAL, INSTRUMENT).

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

  • Premarket exempt
  • Lot / batch number
Other properties (13, all answered No)