Contenitore da 300 ml - SECURBIOP 150 ml + 150 ml FISIO, preriempito con 150ml di formaldeide al 8% rosa e 150ml di soluzione fisiologica. (UDI 08051122870783)
Manufactured by TRACES S.r.l.
Device Regulatory Overview
The Contenitore da 300 ml - SECURBIOP 150 ml + 150 ml FISIO, preriempito con 150ml di formaldeide al 8% rosa e 150ml di soluzione fisiologica. (Model/Catalog Number: SECURBIOP 150+150 FISIO-EOS) 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
- SECURBIOP 150+150 FISIO-EOS
- Product Code / EMDN
- W050301029099
- Device Name
- Contenitore per campioni bioptici
- Database Sync Date
- 2026-08-09 18:40:24
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 Contenitore da 300 ml - SECURBIOP 150 ml + 150 ml FISIO, preriempito con 150ml di formaldeide al 8% rosa e 150ml di soluzione fisiologica.?
The registered manufacturer of record for Contenitore da 300 ml - SECURBIOP 150 ml + 150 ml FISIO, preriempito con 150ml di formaldeide al 8% rosa e 150ml di soluzione fisiologica. is TRACES S.r.l..
What is the Primary UDI-DI identifier for Contenitore da 300 ml - SECURBIOP 150 ml + 150 ml FISIO, preriempito con 150ml di formaldeide al 8% rosa e 150ml di soluzione fisiologica.?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08051122870783.
What classification code is assigned to this device?
This device is registered under product classification code W050301029099.
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Other Devices by TRACES S.r.l.
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