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NatureSpirit CMS50DL

by Simpro

NatureSpirit CMS50DL is a Class II device made by Simpro, listed in FDA GUDID since 28 Jul 2017 (UDI-DI 00897037001212), 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 Number00897037001212 UDI-DI Date28 Jul 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  • Withdrawn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
CMS50DL
Primary DI / UDI-DI
00897037001212
FDA product code
DXN
GMDN term
Pulse oximeter, line-powered
Device class
Class II
Regulation number
870.1130
GUDID distribution status
In Commercial Distribution
MRI safety
MR Safe

Related devices

Category: Pulse oximeter, line-powered

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Properties

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