eudamed_udi
Primary ID: 05907080634000
DESKOROLKA (UDI 05907080634000)
Manufactured by Si-iS Paweł Wyszyński
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DESKOROLKA - Primary ID 05907080634000
Device Regulatory Overview
The DESKOROLKA (Model/Catalog Number: 5907080634000) is a medical device manufactured by Si-iS Paweł Wyszyński. This product is indexed under FDA Product Code / Category Classification Y0599 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 5907080634000
- Product Code / EMDN
- Y0599
- Device Name
- DESKOROLKA
- Database Sync Date
- 2026-08-09 16:51:24
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 DESKOROLKA?
The registered manufacturer of record for DESKOROLKA is Si-iS Paweł Wyszyński.
What is the Primary UDI-DI identifier for DESKOROLKA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05907080634000.
What classification code is assigned to this device?
This device is registered under product classification code Y0599.
Similar Classification Devices (Y0599)
Other Devices by Si-iS Paweł Wyszyński
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