gudid
Primary ID: STP 120-1 SPIN TISSUE
Thermo Fisher (UDI STP 120-1 SPIN TISSUE)
Manufactured by SHANDON DIAGNOSTICS LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Thermo Fisher - Primary ID STP 120-1 SPIN TISSUE
Device Regulatory Overview
The Thermo Fisher (Model/Catalog Number: STP 120-1 SPIN TISSUE) is a medical device manufactured by SHANDON DIAGNOSTICS LIMITED. This product is indexed under FDA Product Code / Category Classification IEO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- STP 120-1 SPIN TISSUE
- Product Code / EMDN
- IEO
- Device Name
- PROCESSOR 100-240V 50/60HZ
- Database Sync Date
- 2026-08-09 09:39:59
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 Thermo Fisher?
The registered manufacturer of record for Thermo Fisher is SHANDON DIAGNOSTICS LIMITED.
What is the Primary UDI-DI identifier for Thermo Fisher?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is STP 120-1 SPIN TISSUE.
What classification code is assigned to this device?
This device is registered under product classification code IEO.
Similar Classification Devices (IEO)
Other Devices by SHANDON DIAGNOSTICS LIMITED
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