Orthopädisches Keilkissen - Art. 202 201 - Schwarz (UDI 04744999460341)
Manufactured by feela., Marco Winter, e-Commerce
Device Regulatory Overview
The Orthopädisches Keilkissen - Art. 202 201 - Schwarz (Model/Catalog Number: 202 201 - Schwarz) is a medical device manufactured by feela., Marco Winter, e-Commerce. This product is indexed under FDA Product Code / Category Classification V080399 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 202 201 - Schwarz
- Product Code / EMDN
- V080399
- Device Name
- Orthopädisches Keilkissen
- Database Sync Date
- 2026-08-09 16:46:10
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 Orthopädisches Keilkissen - Art. 202 201 - Schwarz?
The registered manufacturer of record for Orthopädisches Keilkissen - Art. 202 201 - Schwarz is feela., Marco Winter, e-Commerce.
What is the Primary UDI-DI identifier for Orthopädisches Keilkissen - Art. 202 201 - Schwarz?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04744999460341.
What classification code is assigned to this device?
This device is registered under product classification code V080399.
Similar Classification Devices (V080399)
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