eudamed_udi
Primary ID: 08015262009786
Ago 22GX 11/4"- PENTALANCE (UDI 08015262009786)
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 11/4"- PENTALANCE - Primary ID 08015262009786
Device Regulatory Overview
The Ago 22GX 11/4"- PENTALANCE (Model/Catalog Number: 004021E14) 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
- 004021E14
- Product Code / EMDN
- A0101010102
- Device Name
- SIRINGHE CON AGO E AGHI IPODERMICI
- Database Sync Date
- 2026-08-09 16:29:19
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 Ago 22GX 11/4"- PENTALANCE?
The registered manufacturer of record for Ago 22GX 11/4"- PENTALANCE is PENTAFERTE ITALIA SRL.
What is the Primary UDI-DI identifier for Ago 22GX 11/4"- PENTALANCE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08015262009786.
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
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