NatureSpirit CMS-50F

NatureSpirit CMS-50F is a Class II device made by Simpro, listed in FDA GUDID since 29 Jun 2017 (UDI-DI 00897037001472), 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

Source GUDID, synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	GUDID listing	Number00897037001472 UDI-DI	Date29 Jun 2017Listed	StatusListed GUDID: in commercial distribution

Official records

AccessGUDID record UDI-DI 00897037001472

Coverage

1 jurisdiction

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Withdrawn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-50F

Primary DI / UDI-DI: 00897037001472
FDA product code: DQA
GMDN term: Pulse oximeter, line-powered

Device class: Class II
Regulation number: 870.2700
GUDID distribution status: In Commercial Distribution

MRI safety: MR Safe

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Properties

Over-the-counter
Premarket exempt

Other properties (13, all answered No)