gudid
Primary ID: PF2300NA
PRISMAFLO II S (UDI PF2300NA)
Manufactured by Stihler Electronic GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PRISMAFLO II S - Primary ID PF2300NA
Device Regulatory Overview
The PRISMAFLO II S (Model/Catalog Number: PF2300NA) is a medical device manufactured by Stihler Electronic GmbH. This product is indexed under FDA Product Code / Category Classification KOC within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PF2300NA
- Product Code / EMDN
- KOC
- Device Name
- Blood warmer
- Database Sync Date
- 2026-08-09 09:17:36
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 PRISMAFLO II S?
The registered manufacturer of record for PRISMAFLO II S is Stihler Electronic GmbH.
What is the Primary UDI-DI identifier for PRISMAFLO II S?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PF2300NA.
What classification code is assigned to this device?
This device is registered under product classification code KOC.
Similar Classification Devices (KOC)
Other Devices by Stihler Electronic GmbH
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