eudamed_udi
Primary ID: 00840733102479
Para-Pak® Zn-PVA (UDI 00840733102479)
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® Zn-PVA - Primary ID 00840733102479
Device Regulatory Overview
The Para-Pak® Zn-PVA (Model/Catalog Number: 901012) is a medical device manufactured by Meridian Bioscience Inc.. This product is indexed under FDA Product Code / Category Classification W05019001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 901012
- Product Code / EMDN
- W05019001
- Device Name
- Para-Pak® Zn-PVA
- Database Sync Date
- 2026-08-09 18:14:37
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® Zn-PVA?
The registered manufacturer of record for Para-Pak® Zn-PVA is Meridian Bioscience Inc..
What is the Primary UDI-DI identifier for Para-Pak® Zn-PVA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00840733102479.
What classification code is assigned to this device?
This device is registered under product classification code W05019001.
Similar Classification Devices (W05019001)
Other Devices by Meridian Bioscience Inc.
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