eudamed_udi
Primary ID: 00840733102059
Para-Pak® Ethyl Acetate (UDI 00840733102059)
Manufactured by Meridian Bioscience Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Para-Pak® Ethyl Acetate - Primary ID 00840733102059
Device Regulatory Overview
The Para-Pak® Ethyl Acetate (Model/Catalog Number: FK4318) is a medical device manufactured by Meridian Bioscience Inc.. This product is indexed under FDA Product Code / Category Classification W0104050101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FK4318
- Product Code / EMDN
- W0104050101
- Device Name
- Para-Pak® Ethyl Acetate
- Database Sync Date
- 2026-08-09 17:15:11
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 Para-Pak® Ethyl Acetate?
The registered manufacturer of record for Para-Pak® Ethyl Acetate is Meridian Bioscience Inc..
What is the Primary UDI-DI identifier for Para-Pak® Ethyl Acetate?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00840733102059.
What classification code is assigned to this device?
This device is registered under product classification code W0104050101.
Similar Classification Devices (W0104050101)
Other Devices by Meridian Bioscience Inc.
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