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Medline RTACINDH

by Medline Industries, Inc.

Medline RTACINDH is a Class II device made by Medline Industries, Inc., listed in FDA GUDID since 17 Nov 2021 (UDI-DI 10193489080513), 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 Number10193489080513 UDI-DI Date17 Nov 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  • Withdrawn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
Medline
Generic name
Vacuum suction regulator/regulation set, general-purpose
Model / Ref / Catalog
RTACINDH
Primary DI / UDI-DI
10193489080513
FDA product code
KDP
GMDN term
Vacuum suction regulator/regulation set, general-purpose
Device class
Class II
Regulation number
880.6740
GUDID distribution status
In Commercial Distribution

Related devices

Category: Vacuum suction regulator/regulation set, general-purpose

Similar devices

Other devices filed under FDA product code KDP (REGULATOR, VACUUM).

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

  • Prescription use
  • Premarket exempt
  • Serial number
Other properties (12, all answered No)