Siringa 50 ml luer lock (amber)- PENTA (UDI 08015262020941)
Manufactured by PENTAFERTE ITALIA SRL
Device Regulatory Overview
The Siringa 50 ml luer lock (amber)- PENTA (Model/Catalog Number: 002022920AF) is a medical device manufactured by PENTAFERTE ITALIA SRL. This product is indexed under FDA Product Code / Category Classification A020102020102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 002022920AF
- Product Code / EMDN
- A020102020102
- Device Name
- SIRINGHE ED ACCESSORI PER POMPE D'INFUSIONE
- Database Sync Date
- 2026-08-09 17:00:07
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 50 ml luer lock (amber)- PENTA?
The registered manufacturer of record for Siringa 50 ml luer lock (amber)- PENTA is PENTAFERTE ITALIA SRL.
What is the Primary UDI-DI identifier for Siringa 50 ml luer lock (amber)- PENTA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08015262020941.
What classification code is assigned to this device?
This device is registered under product classification code A020102020102.
Similar Classification Devices (A020102020102)
Other Devices by PENTAFERTE ITALIA SRL
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