gudid
Primary ID: Sanibel REM Probe Tubes, type D
Sanibel Supply A/S (UDI Sanibel REM Probe Tubes, type D)
Manufactured by Interacoustics A/S
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sanibel Supply A/S - Primary ID Sanibel REM Probe Tubes, type D
Device Regulatory Overview
The Sanibel Supply A/S (Model/Catalog Number: Sanibel REM Probe Tubes, type D) is a medical device manufactured by Interacoustics A/S. This product is indexed under FDA Product Code / Category Classification ETW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Sanibel REM Probe Tubes, type D
- Product Code / EMDN
- ETW
- Device Name
- Accessory for Real Ear Measurement (REM), red
- Database Sync Date
- 2026-08-09 09:12:46
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Sanibel Supply A/S?
The registered manufacturer of record for Sanibel Supply A/S is Interacoustics A/S.
What is the Primary UDI-DI identifier for Sanibel Supply A/S?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Sanibel REM Probe Tubes, type D.
What classification code is assigned to this device?
This device is registered under product classification code ETW.
Similar Classification Devices (ETW)
Other Devices by Interacoustics A/S
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