eudamed_udi
Primary ID: 08437024657019
HANK (UDI 08437024657019)
Manufactured by Gogoa Mobility Robots
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HANK - Primary ID 08437024657019
Device Regulatory Overview
The HANK (Model/Catalog Number: HANKV2.1) is a medical device manufactured by Gogoa Mobility Robots. This product is indexed under FDA Product Code / Category Classification Y061218 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HANKV2.1
- Product Code / EMDN
- Y061218
- Device Name
- HANK
- Database Sync Date
- 2026-08-09 16:48:10
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 HANK?
The registered manufacturer of record for HANK is Gogoa Mobility Robots.
What is the Primary UDI-DI identifier for HANK?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08437024657019.
What classification code is assigned to this device?
This device is registered under product classification code Y061218.
Similar Classification Devices (Y061218)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint