eudamed_udi
Primary ID: 08906085430126
Nihal (UDI 08906085430126)
Manufactured by Nihal Healthcare
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Nihal - Primary ID 08906085430126
Device Regulatory Overview
The Nihal (Model/Catalog Number: 8906085430126) is a medical device manufactured by Nihal Healthcare. This product is indexed under FDA Product Code / Category Classification A020102010202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 8906085430126
- Product Code / EMDN
- A020102010202
- Device Name
- Sterile Hypodermic Syringe without Needle
- Database Sync Date
- 2026-08-09 16:47:55
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 Nihal?
The registered manufacturer of record for Nihal is Nihal Healthcare.
What is the Primary UDI-DI identifier for Nihal?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08906085430126.
What classification code is assigned to this device?
This device is registered under product classification code A020102010202.
Similar Classification Devices (A020102010202)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint