eudamed_udi
Primary ID: 08903545072926
Anina Safety (UDI 08903545072926)
Manufactured by Global Medikit Limited
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Anina Safety - Primary ID 08903545072926
Device Regulatory Overview
The Anina Safety (Model/Catalog Number: 4046162) is a medical device manufactured by Global Medikit Limited. This product is indexed under FDA Product Code / Category Classification C0101010201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4046162
- Product Code / EMDN
- C0101010201
- Device Name
- I.V. Catheter
- Database Sync Date
- 2026-08-09 16:30:02
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 Anina Safety?
The registered manufacturer of record for Anina Safety is Global Medikit Limited.
What is the Primary UDI-DI identifier for Anina Safety?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08903545072926.
What classification code is assigned to this device?
This device is registered under product classification code C0101010201.
Similar Classification Devices (C0101010201)
Other Devices by Global Medikit Limited
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint