GUDIDData
eudamed_udi Primary ID: 08015262021177

Siringa 2,5 ml con ago 22GX 11/4"- PENTA (UDI 08015262021177)

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 con ago 22GX 11/4"- PENTA - Primary ID 08015262021177

Device Regulatory Overview

The Siringa 2,5 ml con ago 22GX 11/4"- PENTA (Model/Catalog Number: 00202230E14) is a medical device manufactured by PENTAFERTE ITALIA SRL. This product is indexed under FDA Product Code / Category Classification A020102010201 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
00202230E14
Product Code / EMDN
A020102010201
Device Name
SIRINGHE CON AGO E AGHI IPODERMICI
Database Sync Date
2026-08-09 16:48:13

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Siringa 2,5 ml con ago 22GX 11/4"- PENTA?

The registered manufacturer of record for Siringa 2,5 ml con ago 22GX 11/4"- PENTA is PENTAFERTE ITALIA SRL.

What is the Primary UDI-DI identifier for Siringa 2,5 ml con ago 22GX 11/4"- PENTA?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08015262021177.

What classification code is assigned to this device?

This device is registered under product classification code A020102010201.

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