eudamed_udi
Primary ID: 08015262009762
Ago 22GX 1"- PENTALANCE (UDI 08015262009762)
Manufactured by PENTAFERTE ITALIA SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Ago 22GX 1"- PENTALANCE - Primary ID 08015262009762
Device Regulatory Overview
The Ago 22GX 1"- PENTALANCE (Model/Catalog Number: 004021E10) is a medical device manufactured by PENTAFERTE ITALIA SRL. This product is indexed under FDA Product Code / Category Classification A0101010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 004021E10
- Product Code / EMDN
- A0101010102
- Device Name
- SIRINGHE CON AGO E AGHI IPODERMICI
- Database Sync Date
- 2026-08-09 16:49:12
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Ago 22GX 1"- PENTALANCE?
The registered manufacturer of record for Ago 22GX 1"- PENTALANCE is PENTAFERTE ITALIA SRL.
What is the Primary UDI-DI identifier for Ago 22GX 1"- PENTALANCE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08015262009762.
What classification code is assigned to this device?
This device is registered under product classification code A0101010102.
Similar Classification Devices (A0101010102)
Other Devices by PENTAFERTE ITALIA SRL
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint