FERRITINA CALIBRADOR (UDI 18430155003158)
Manufactured by QUIMICA CLINICA APLICADA S.A.
Device Regulatory Overview
The FERRITINA CALIBRADOR (Model/Catalog Number: 992130) is a medical device manufactured by QUIMICA CLINICA APLICADA S.A.. This product is indexed under FDA Product Code / Category Classification W0102152206 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 992130
- Product Code / EMDN
- W0102152206
- Device Name
- FERRITINA CALIBRADOR
- Database Sync Date
- 2026-08-09 18:37:11
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 FERRITINA CALIBRADOR?
The registered manufacturer of record for FERRITINA CALIBRADOR is QUIMICA CLINICA APLICADA S.A..
What is the Primary UDI-DI identifier for FERRITINA CALIBRADOR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 18430155003158.
What classification code is assigned to this device?
This device is registered under product classification code W0102152206.
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Other Devices by QUIMICA CLINICA APLICADA S.A.
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