DeoMed Bamboo (UDI 05901050914666)
Manufactured by JJW Spółka Jawna J. Karpiński, J. Rudnicki, W. Lewin
Device Regulatory Overview
The DeoMed Bamboo (Model/Catalog Number: DMB) 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
- DMB
- Product Code / EMDN
- Y0999
- Device Name
- Skarpetki zdrowotne profilaktyczne
- Database Sync Date
- 2026-08-09 16:44:55
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 DeoMed Bamboo?
The registered manufacturer of record for DeoMed Bamboo is JJW Spółka Jawna J. Karpiński, J. Rudnicki, W. Lewin.
What is the Primary UDI-DI identifier for DeoMed Bamboo?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05901050914666.
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
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