gudid
Primary ID: 00951
Asserachrom PF4 (UDI 00951)
Manufactured by DIAGNOSTICA STAGO
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Asserachrom PF4 - Primary ID 00951
Device Regulatory Overview
The Asserachrom PF4 (Model/Catalog Number: 00951) is a medical device manufactured by DIAGNOSTICA STAGO. This product is indexed under FDA Product Code / Category Classification LCO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 00951
- Product Code / EMDN
- LCO
- Device Name
- Database Sync Date
- 2026-08-09 09:23:29
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 Asserachrom PF4?
The registered manufacturer of record for Asserachrom PF4 is DIAGNOSTICA STAGO.
What is the Primary UDI-DI identifier for Asserachrom PF4?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00951.
What classification code is assigned to this device?
This device is registered under product classification code LCO.
Similar Classification Devices (LCO)
Other Devices by DIAGNOSTICA STAGO
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