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Sanibel Supply EarTurtle, Slide

by Interacoustics A/S

Sanibel Supply EarTurtle, Slide is a Class I device made by Interacoustics A/S, listed in FDA GUDID since 8 Dec 2022 (UDI-DI 05711117225594), 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 Number05711117225594 UDI-DI Date8 Dec 2022ListedStatusListed 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  • Withdrawn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
Sanibel Supply
Generic name
Earphone cushion
Model / reference
EarTurtle, Slide
Primary DI / UDI-DI
05711117225594
FDA product code
ETT
GMDN term
Earphone cushion
Device class
Class I
Regulation number
874.1100
GUDID distribution status
In Commercial Distribution

Related devices

Category: Earphone cushion

Similar devices

Other devices filed under FDA product code ETT (Cushion, Earphone (For Audiometric Testing)).

Other devices from Interacoustics A/S

See all devices from Interacoustics A/S →

Properties

  • Single use
  • Premarket exempt
  • Lot / batch number
  • Expiration date
Other properties (11, all answered No)