DEOMED WOOL (UDI 05901050202824)
Manufactured by JJW Spółka Jawna J. Karpiński, J. Rudnicki, W. Lewin
Device Regulatory Overview
The DEOMED WOOL (Model/Catalog Number: DMW) is a medical device manufactured by JJW Spółka Jawna J. Karpiński, J. Rudnicki, W. Lewin. This product is indexed under FDA Product Code / Category Classification Y0999 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DMW
- Product Code / EMDN
- Y0999
- Device Name
- Skarpetki zdrowotne profilaktyczne
- Database Sync Date
- 2026-08-09 16:50:23
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of DEOMED WOOL?
The registered manufacturer of record for DEOMED WOOL is JJW Spółka Jawna J. Karpiński, J. Rudnicki, W. Lewin.
What is the Primary UDI-DI identifier for DEOMED WOOL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05901050202824.
What classification code is assigned to this device?
This device is registered under product classification code Y0999.
Similar Classification Devices (Y0999)
Other Devices by JJW Spółka Jawna J. Karpiński, J. Rudnicki, W. Lewin
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint