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Andesfit ADF-B06

by Andesfit Limited

Andesfit ADF-B06 is a Class II device made by Andesfit Limited, listed in FDA GUDID since 9 May 2019 (UDI-DI 00146191200604), 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 Number00146191200604 UDI-DI Date9 May 2019ListedStatusListed 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  • Withdrawn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
Andesfit
Generic name
Pulse oximeter
Model / reference
ADF-B06
Primary DI / UDI-DI
00146191200604
FDA product code
DQA
GMDN term
Pulse oximeter
Device class
Class II
Regulation number
870.2700
GUDID distribution status
In Commercial Distribution

Related devices

Category: Pulse oximeter

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Other devices filed under Pulse oximeter.

Other devices from Andesfit Limited

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Properties

  • Lot / batch number
  • Manufacturing date
Other properties (13, all answered No)