eudamed_udi
Primary ID: 04251931380198
Patientendrehhilfe (UDI 04251931380198)
Manufactured by Bisanz medizinische Polster GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Patientendrehhilfe - Primary ID 04251931380198
Device Regulatory Overview
The Patientendrehhilfe (Model/Catalog Number: 460901) is a medical device manufactured by Bisanz medizinische Polster GmbH. This product is indexed under FDA Product Code / Category Classification V080302 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 460901
- Product Code / EMDN
- V080302
- Device Name
- Patientendrehhilfe
- Database Sync Date
- 2026-08-09 16:29:49
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 Patientendrehhilfe?
The registered manufacturer of record for Patientendrehhilfe is Bisanz medizinische Polster GmbH.
What is the Primary UDI-DI identifier for Patientendrehhilfe?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251931380198.
What classification code is assigned to this device?
This device is registered under product classification code V080302.
Similar Classification Devices (V080302)
Other Devices by Bisanz medizinische Polster GmbH
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