eudamed_udi
Primary ID: 03800232427517
Gripper kit (UDI 03800232427517)
Manufactured by STS Medical Group AD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Gripper kit - Primary ID 03800232427517
Device Regulatory Overview
The Gripper kit (Model/Catalog Number: 20030) is a medical device manufactured by STS Medical Group AD. This product is indexed under FDA Product Code / Category Classification V0502 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 20030
- Product Code / EMDN
- V0502
- Device Name
- Injection / Infusion, Non sterile
- Database Sync Date
- 2026-08-09 16:46:29
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 Gripper kit?
The registered manufacturer of record for Gripper kit is STS Medical Group AD.
What is the Primary UDI-DI identifier for Gripper kit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 03800232427517.
What classification code is assigned to this device?
This device is registered under product classification code V0502.
Similar Classification Devices (V0502)
Other Devices by STS Medical Group AD
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint