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Medline MDSLS4LOP

by Medline Industries, Inc.

Medline MDSLS4LOP is a Class II device made by Medline Industries, Inc., listed in FDA GUDID since 9 Sep 2024 (UDI-DI 10193489136210), 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 Number10193489136210 UDI-DI Date9 Sep 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  • Withdrawn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
Ophthalmic/otologic diagnostic set
Model / Ref / Catalog
MDSLS4LOP
Primary DI / UDI-DI
10193489136210
FDA product code
HLJ
GMDN term
Ophthalmic/otologic diagnostic set
Device class
Class II
Regulation number
886.1570
GUDID distribution status
In Commercial Distribution
MRI safety
MR Unsafe

Related devices

Category: Ophthalmic/otologic diagnostic set

Similar devices

Other devices filed under FDA product code HLJ (Ophthalmoscope, battery-powered).

Other devices from Medline Industries, Inc.

See all devices from Medline Industries, Inc. →

Properties

  • Prescription use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)