GUDIDData
eudamed_udi Primary ID: 89640033151392

Amject AD Syringe 5ml with Needle (UDI 89640033151392)

Manufactured by Amson Vaccines & Pharma (Pvt) Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Amject AD Syringe 5ml with Needle - Primary ID 89640033151392

Device Regulatory Overview

The Amject AD Syringe 5ml with Needle (Model/Catalog Number: 06-06-0004) is a medical device manufactured by Amson Vaccines & Pharma (Pvt) Ltd.. This product is indexed under FDA Product Code / Category Classification A020199 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
06-06-0004
Product Code / EMDN
A020199
Device Name
Amject AD Syringe 5ml with Needle
Database Sync Date
2026-08-09 16:48:02

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 Amject AD Syringe 5ml with Needle?

The registered manufacturer of record for Amject AD Syringe 5ml with Needle is Amson Vaccines & Pharma (Pvt) Ltd..

What is the Primary UDI-DI identifier for Amject AD Syringe 5ml with Needle?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 89640033151392.

What classification code is assigned to this device?

This device is registered under product classification code A020199.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint