eudamed_udi
Primary ID: 06975090503257
Unspecified Brand (UDI 06975090503257)
Manufactured by Accucise Diagnostics Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 06975090503257
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 1020312000) is a medical device manufactured by Accucise Diagnostics Inc.. This product is indexed under FDA Product Code / Category Classification W0102069013 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1020312000
- Product Code / EMDN
- W0102069013
- Device Name
- Procalcitonin STAT (EECL)
- Database Sync Date
- 2026-08-09 16:47:01
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Accucise Diagnostics Inc..
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975090503257.
What classification code is assigned to this device?
This device is registered under product classification code W0102069013.
Similar Classification Devices (W0102069013)
Other Devices by Accucise Diagnostics Inc.
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