eudamed_udi
Primary ID: 16438153000713
sTfR Calibration Set (UDI 16438153000713)
Manufactured by Thermo Fisher Scientific Oy
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for sTfR Calibration Set - Primary ID 16438153000713
Device Regulatory Overview
The sTfR Calibration Set (Model/Catalog Number: 981865) is a medical device manufactured by Thermo Fisher Scientific Oy. This product is indexed under FDA Product Code / Category Classification W0102152206 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 981865
- Product Code / EMDN
- W0102152206
- Device Name
- sTfR Calibration Set
- Database Sync Date
- 2026-08-09 16:50:43
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 sTfR Calibration Set?
The registered manufacturer of record for sTfR Calibration Set is Thermo Fisher Scientific Oy.
What is the Primary UDI-DI identifier for sTfR Calibration Set?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 16438153000713.
What classification code is assigned to this device?
This device is registered under product classification code W0102152206.
Similar Classification Devices (W0102152206)
Other Devices by Thermo Fisher Scientific Oy
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