eudamed_udi
Primary ID: 08055348434095
Unspecified Brand (UDI 08055348434095)
Manufactured by Meika Group S.r.l.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 08055348434095
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: CRO2001) is a medical device manufactured by Meika Group S.r.l.. This product is indexed under FDA Product Code / Category Classification K0104 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CRO2001
- Product Code / EMDN
- K0104
- Device Name
- AGO di VERRES 14 GA 100 mm
- Database Sync Date
- 2026-08-09 17:34:11
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Meika Group S.r.l..
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08055348434095.
What classification code is assigned to this device?
This device is registered under product classification code K0104.
Similar Classification Devices (K0104)
Other Devices by Meika Group S.r.l.
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