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Sanibel Supply A/S

FDA UDI

Class II (US FDA UDI)

by Interacoustics A/S

Identity

Trade Name
Sanibel Supply A/S FDA UDI
Generic Name
Audiometric/hearing aid tester FDA UDI
Device Name
Accessory for Real Ear Measurement (REM), black FDA UDI
Model / Reference
Sanibel REM Probe Tubes, type A FDA UDI
Description
Accessory for Real Ear Measurement (REM), black FDA UDI

Identifiers

Catalog Number
8533301 (50 pcs) FDA UDI
Primary DI / UDI-DI
05711117227550 FDA UDI
FDA Product Code
ETW FDA UDI
GMDN Term
Audiometric/hearing aid tester FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
874.3310 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

Yes

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Audiometric/hearing aid tester

Sanibel Supply A/S by Interacoustics A/S — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Audiometric/hearing aid tester.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Interacoustics A/S

Sources (1)

  • FDA UDI 63c9b005-793e-4839-974b-82edc45e1481 34 fields · synced Jun 8, 2026