eudamed_udi
Primary ID: D-029908-8461-8430-357GG
ThinTube (UDI D-029908-8461-8430-357GG)
Manufactured by audifon GmbH & Co. KG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ThinTube - Primary ID D-029908-8461-8430-357GG
Device Regulatory Overview
The ThinTube (Model/Catalog Number: 029908-8461-8430-357) is a medical device manufactured by audifon GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification Y214580 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 029908-8461-8430-357
- Product Code / EMDN
- Y214580
- Device Name
- Sound tube
- Database Sync Date
- 2026-08-09 16:28:54
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 ThinTube?
The registered manufacturer of record for ThinTube is audifon GmbH & Co. KG.
What is the Primary UDI-DI identifier for ThinTube?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-029908-8461-8430-357GG.
What classification code is assigned to this device?
This device is registered under product classification code Y214580.
Similar Classification Devices (Y214580)
Other Devices by audifon GmbH & Co. KG
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