RONDELLA PER VITE CON TESTA Ø2.5MM ØESTERNO 5.0MM ST (UDI 08055400678818)
Manufactured by Mikai s.p.a.
Device Regulatory Overview
The RONDELLA PER VITE CON TESTA Ø2.5MM ØESTERNO 5.0MM ST (Model/Catalog Number: BTR25005WST) is a medical device manufactured by Mikai s.p.a.. This product is indexed under FDA Product Code / Category Classification P091280 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BTR25005WST
- Product Code / EMDN
- P091280
- Device Name
- BSS
- Database Sync Date
- 2026-08-09 16:49:17
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 RONDELLA PER VITE CON TESTA Ø2.5MM ØESTERNO 5.0MM ST?
The registered manufacturer of record for RONDELLA PER VITE CON TESTA Ø2.5MM ØESTERNO 5.0MM ST is Mikai s.p.a..
What is the Primary UDI-DI identifier for RONDELLA PER VITE CON TESTA Ø2.5MM ØESTERNO 5.0MM ST?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08055400678818.
What classification code is assigned to this device?
This device is registered under product classification code P091280.
Similar Classification Devices (P091280)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint