eudamed_udi
Primary ID: 04004128031393
Beckenbodentrainer SGL (UDI 04004128031393)
Manufactured by Hydas GmbH & Co. KG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Beckenbodentrainer SGL - Primary ID 04004128031393
Device Regulatory Overview
The Beckenbodentrainer SGL (Model/Catalog Number: 9681.1.00) is a medical device manufactured by Hydas GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification T0499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 9681.1.00
- Product Code / EMDN
- T0499
- Device Name
- Beckenbodentrainer
- Database Sync Date
- 2026-08-09 16:28:44
Full Regulatory Attributes
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{
"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 Beckenbodentrainer SGL?
The registered manufacturer of record for Beckenbodentrainer SGL is Hydas GmbH & Co. KG.
What is the Primary UDI-DI identifier for Beckenbodentrainer SGL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04004128031393.
What classification code is assigned to this device?
This device is registered under product classification code T0499.
Similar Classification Devices (T0499)
Other Devices by Hydas GmbH & Co. KG
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