eudamed_udi
Primary ID: 18053326001632
eNAT (UDI 18053326001632)
Manufactured by Copan Italia S.P.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for eNAT - Primary ID 18053326001632
Device Regulatory Overview
The eNAT (Model/Catalog Number: 606CS01M) is a medical device manufactured by Copan Italia S.P.A.. This product is indexed under FDA Product Code / Category Classification A1102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 606CS01M
- Product Code / EMDN
- A1102
- Device Name
- 2 ML PRESERVATION MEDIUM FOR NUCLEIC ACIDS MINITIP FL. APPLIC.
- Database Sync Date
- 2026-08-09 16:29:10
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 eNAT?
The registered manufacturer of record for eNAT is Copan Italia S.P.A..
What is the Primary UDI-DI identifier for eNAT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 18053326001632.
What classification code is assigned to this device?
This device is registered under product classification code A1102.
Similar Classification Devices (A1102)
Other Devices by Copan Italia S.P.A.
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