FERRITIN CALIBRATOR (UDI 08033622173274)
Manufactured by BEN S.R.L. BIOCHEMICAL ENTERPRISE
Device Regulatory Overview
The FERRITIN CALIBRATOR (Model/Catalog Number: FEST6201) is a medical device manufactured by BEN S.R.L. BIOCHEMICAL ENTERPRISE. This product is indexed under FDA Product Code / Category Classification W0102152206 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FEST6201
- Product Code / EMDN
- W0102152206
- Device Name
- FERRITIN CALIBRATOR
- Database Sync Date
- 2026-08-09 18:39:40
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 FERRITIN CALIBRATOR?
The registered manufacturer of record for FERRITIN CALIBRATOR is BEN S.R.L. BIOCHEMICAL ENTERPRISE.
What is the Primary UDI-DI identifier for FERRITIN CALIBRATOR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08033622173274.
What classification code is assigned to this device?
This device is registered under product classification code W0102152206.
Similar Classification Devices (W0102152206)
Other Devices by BEN S.R.L. BIOCHEMICAL ENTERPRISE
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