K40 10+10.Contenitore per campioni bioptici preriempito con 10ml formaldeide 8% e 10ml soluzione fisiologica (UDI 08051122871438)
Manufactured by TRACES S.r.l.
Device Regulatory Overview
The K40 10+10.Contenitore per campioni bioptici preriempito con 10ml formaldeide 8% e 10ml soluzione fisiologica (Model/Catalog Number: AA10+10K40) is a medical device manufactured by TRACES S.r.l.. This product is indexed under FDA Product Code / Category Classification W050301029099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AA10+10K40
- Product Code / EMDN
- W050301029099
- Device Name
- Contenitore per campioni bioptici
- Database Sync Date
- 2026-08-09 17:20:34
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 K40 10+10.Contenitore per campioni bioptici preriempito con 10ml formaldeide 8% e 10ml soluzione fisiologica?
The registered manufacturer of record for K40 10+10.Contenitore per campioni bioptici preriempito con 10ml formaldeide 8% e 10ml soluzione fisiologica is TRACES S.r.l..
What is the Primary UDI-DI identifier for K40 10+10.Contenitore per campioni bioptici preriempito con 10ml formaldeide 8% e 10ml soluzione fisiologica?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08051122871438.
What classification code is assigned to this device?
This device is registered under product classification code W050301029099.
Similar Classification Devices (W050301029099)
Other Devices by TRACES S.r.l.
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