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Medline MDS096204P

by Medline Industries, Inc.

Medline MDS096204P is a Class II device made by Medline Industries, Inc., listed in FDA GUDID since 8 Jul 2024 (UDI-DI 80888277102988), 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 Number80888277102988 UDI-DI Date8 Jul 2024ListedStatusListed 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  • Withdrawn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
Surgical/emergency suction cannula, non-illuminating, single-use
Model / Ref / Catalog
MDS096204P
Primary DI / UDI-DI
80888277102988
FDA product code
JOL
GMDN term
Surgical/emergency suction cannula, non-illuminating, single-use
Device class
Class II
Regulation number
880.6740
GUDID distribution status
In Commercial Distribution

Related devices

Category: Surgical/emergency suction cannula, non-illuminating, single-useOral care swab

Similar devices

Also classified as Oral care swab.

Similar devices

Other devices filed under FDA product code JOL (CATHETER AND TIP, SUCTION).

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

  • Single use
  • Over-the-counter
  • Premarket exempt
  • Lot / batch number
Other properties (11, all answered No)