eudamed_udi
Primary ID: 08015262022020
Siringa 2,5 ml SLIP- NEURAFIT (UDI 08015262022020)
Manufactured by PENTAFERTE ITALIA SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Siringa 2,5 ml SLIP- NEURAFIT - Primary ID 08015262022020
Device Regulatory Overview
The Siringa 2,5 ml SLIP- NEURAFIT (Model/Catalog Number: V051010031A1) is a medical device manufactured by PENTAFERTE ITALIA SRL. This product is indexed under FDA Product Code / Category Classification A02010299 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- V051010031A1
- Product Code / EMDN
- A02010299
- Device Name
- SIRINGHE SENZA AGO ED ACCESSORI
- Database Sync Date
- 2026-08-09 17:08:46
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 Siringa 2,5 ml SLIP- NEURAFIT?
The registered manufacturer of record for Siringa 2,5 ml SLIP- NEURAFIT is PENTAFERTE ITALIA SRL.
What is the Primary UDI-DI identifier for Siringa 2,5 ml SLIP- NEURAFIT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08015262022020.
What classification code is assigned to this device?
This device is registered under product classification code A02010299.
Similar Classification Devices (A02010299)
Other Devices by PENTAFERTE ITALIA SRL
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