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Medline MDS7PLG1

by Medline Industries, Inc.

Medline MDS7PLG1 is a Class II device made by Medline Industries, Inc., listed in FDA GUDID since 6 Sep 2023 (UDI-DI 20193489144809), 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 Number20193489144809 UDI-DI Date6 Sep 2023ListedStatusListed 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  • Withdrawn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
Ligation clip, synthetic polymer, non-bioabsorbable
Model / Ref / Catalog
MDS7PLG1
Primary DI / UDI-DI
20193489144809
FDA product code
FZP
GMDN term
Ligation clip, synthetic polymer, non-bioabsorbable
Device class
Class II
Regulation number
878.4300
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe

Related devices

Category: Ligation clip, synthetic polymer, non-bioabsorbable

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

  • Supplied sterile
  • Single use
  • Implantable
  • Prescription use
  • Lot / batch number
  • Expiration date
Other properties (9, all answered No)