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ProHT JPD-500E

by Inland Products, Inc.

ProHT JPD-500E is a Class II device made by Inland Products, Inc., listed in FDA GUDID since 17 Aug 2016 (UDI-DI 00012405890032), 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 Number00012405890032 UDI-DI Date17 Aug 2016ListedStatusListed 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  • Withdrawn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
ProHT
Generic name
Pulse oximeter, line-powered
Model / reference
JPD-500E
Primary DI / UDI-DI
00012405890032
FDA product code
OCH
GMDN term
Pulse oximeter, line-powered
Device class
Class II
Regulation number
870.2700
GUDID distribution status
In Commercial Distribution

Related devices

Category: Pulse oximeter, line-powered

Similar devices in this category

Other devices filed under Pulse oximeter, line-powered.

Other devices from Inland Products, Inc.

  • ProHT JPD-FR401

    Class II

Properties

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