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Sanibel Supply

FDA UDI

Class I (US FDA UDI)

by Interacoustics A/S

Identity

Trade Name
Sanibel Supply FDA UDI
Generic Name
Vestibulo-auditory analysis system support kit¿ FDA UDI
Model / Reference
ADI eartip sample kit, E3 FDA UDI

Identifiers

Primary DI / UDI-DI
05711117223101 FDA UDI
FDA Product Code
ETT FDA UDI
GMDN Term
Vestibulo-auditory analysis system support kit¿ FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
874.1100 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

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Vestibulo-auditory analysis system support kit¿

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

Similar devices

Also classified as Vestibulo-auditory analysis system support kit¿.

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 b8e0db64-ff1b-46bf-9452-082992f9823d 32 fields · synced May 30, 2026