Schaumstoffkissen (UDI 04251931328329)
Manufactured by Bisanz medizinische Polster GmbH
Device Regulatory Overview
The Schaumstoffkissen (Model/Catalog Number: 300075KLanti) 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
- 300075KLanti
- Product Code / EMDN
- V080302
- Device Name
- Universelle Lagerungskissen
- Database Sync Date
- 2026-08-09 16:29:14
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 Schaumstoffkissen?
The registered manufacturer of record for Schaumstoffkissen is Bisanz medizinische Polster GmbH.
What is the Primary UDI-DI identifier for Schaumstoffkissen?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04251931328329.
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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