eudamed_udi
Primary ID: 04251929221915
Armwechselbad Kneipp (UDI 04251929221915)
Manufactured by Unbescheiden GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Armwechselbad Kneipp - Primary ID 04251929221915
Device Regulatory Overview
The Armwechselbad Kneipp (Model/Catalog Number: 2.19-1) is a medical device manufactured by Unbescheiden GmbH. This product is indexed under FDA Product Code / Category Classification Z120618 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2.19-1
- Product Code / EMDN
- Z120618
- Device Name
- Wechselteilbäder
- Database Sync Date
- 2026-08-09 16:47:01
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 Armwechselbad Kneipp?
The registered manufacturer of record for Armwechselbad Kneipp is Unbescheiden GmbH.
What is the Primary UDI-DI identifier for Armwechselbad Kneipp?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251929221915.
What classification code is assigned to this device?
This device is registered under product classification code Z120618.
Similar Classification Devices (Z120618)
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