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NatureSpirit Sonoline B

by Simpro

NatureSpirit Sonoline B is a Class II device made by Simpro, listed in FDA GUDID since 9 Jun 2017 (UDI-DI 00897037001144), 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 Number00897037001144 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  • Withdrawn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
Foetal Doppler system
Model / reference
Sonoline B
Primary DI / UDI-DI
00897037001144
FDA product code
KNG
GMDN term
Foetal Doppler system
Device class
Class II
Regulation number
884.2660
GUDID distribution status
In Commercial Distribution

Related devices

Category: Foetal Doppler system

Similar devices in this category

Other devices filed under Foetal Doppler system.

Other devices from Simpro

See all devices from Simpro →

Properties

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