eudamed_udi
Primary ID: 08015262036249
Unspecified Brand (UDI 08015262036249)
Manufactured by PENTAFERTE ITALIA SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 08015262036249
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 02452101) is a medical device manufactured by PENTAFERTE ITALIA SRL. This product is indexed under FDA Product Code / Category Classification U03010201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 02452101
- Product Code / EMDN
- U03010201
- Device Name
- Applicatore uretrale
- Database Sync Date
- 2026-08-09 17:05:19
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 PENTAFERTE ITALIA SRL.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08015262036249.
What classification code is assigned to this device?
This device is registered under product classification code U03010201.
Similar Classification Devices (U03010201)
Other Devices by PENTAFERTE ITALIA SRL
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