CATHULA+ (UDI 18903347039476)
Manufactured by Hindustan Syringes & Medical Devices Ltd.
Device Regulatory Overview
The CATHULA+ (Model/Catalog Number: 03947) is a medical device manufactured by Hindustan Syringes & Medical Devices Ltd.. This product is indexed under FDA Product Code / Category Classification C0101010201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 03947
- Product Code / EMDN
- C0101010201
- Device Name
- Intravenous Cannula (I V Cannula)
- Database Sync Date
- 2026-08-09 16:29:24
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 CATHULA+?
The registered manufacturer of record for CATHULA+ is Hindustan Syringes & Medical Devices Ltd..
What is the Primary UDI-DI identifier for CATHULA+?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 18903347039476.
What classification code is assigned to this device?
This device is registered under product classification code C0101010201.
Similar Classification Devices (C0101010201)
Other Devices by Hindustan Syringes & Medical Devices Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint