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Hls 1300

by Healthcare Logistics Systems

Hls 1300 is a Class II device made by Healthcare Logistics Systems, listed in FDA GUDID since 6 Jan 2026 (UDI-DI 00817698020728), registry data as of 22 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 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesGUDID listing Number00817698020728 UDI-DI Date6 Jan 2026ListedStatusListed 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  • Withdrawn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
Hls
Generic name
Pulse oximeter
Model / reference
1300
Primary DI / UDI-DI
00817698020728
FDA product code
DQA
GMDN term
Pulse oximeter
Device class
Class II
Regulation number
870.2700
GUDID distribution status
In Commercial Distribution

Other devices from Healthcare Logistics Systems

See all devices from Healthcare Logistics Systems →

Properties

  • Lot / batch number
  • Serial number
  • Manufacturing date
Other properties (12, all answered No)