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NatureSpirit CMS-50dl

by Simpro

NatureSpirit CMS-50dl is a Class II device made by Simpro, listed in FDA GUDID since 9 Jun 2017 (UDI-DI 00897037001083), 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 Number00897037001083 UDI-DI Date9 Jun 2017ListedStatusListed 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  • Withdrawn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
NatureSpirit
Generic name
Pulse oximeter, line-powered
Model / reference
CMS-50dl
Primary DI / UDI-DI
00897037001083
FDA product code
DQA
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

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Other devices filed under Pulse oximeter, line-powered.

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Properties

  • Over-the-counter
  • Premarket exempt
Other properties (13, all answered No)