High pressure injection/aspiration system for syringe - Connector H (UDI AK-0383/H2)
Manufactured by AKTIVE SRL
Device Regulatory Overview
The High pressure injection/aspiration system for syringe - Connector H (Model/Catalog Number: AK-0383/H2) is a medical device manufactured by AKTIVE SRL. This product is indexed under FDA Product Code / Category Classification KYG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AK-0383/H2
- Product Code / EMDN
- KYG
- Device Name
- High pressure injection/aspiration system for syringe - Connector H
- Database Sync Date
- 2026-08-09 09:04:32
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 High pressure injection/aspiration system for syringe - Connector H?
The registered manufacturer of record for High pressure injection/aspiration system for syringe - Connector H is AKTIVE SRL.
What is the Primary UDI-DI identifier for High pressure injection/aspiration system for syringe - Connector H?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is AK-0383/H2.
What classification code is assigned to this device?
This device is registered under product classification code KYG.
Similar Classification Devices (KYG)
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