eudamed_udi
Primary ID: 01220000531765
DONJOY NEXTEP WALKER (UDI 01220000531765)
Manufactured by Span Link International, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DONJOY NEXTEP WALKER - Primary ID 01220000531765
Device Regulatory Overview
The DONJOY NEXTEP WALKER (Model/Catalog Number: 82-118-S) is a medical device manufactured by Span Link International, LLC. This product is indexed under FDA Product Code / Category Classification Y06120601 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 82-118-S
- Product Code / EMDN
- Y06120601
- Device Name
- DONJOY NEXTEP WALKER
- Database Sync Date
- 2026-08-09 16:48:30
Full Regulatory Attributes
đź”’ 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 DONJOY NEXTEP WALKER?
The registered manufacturer of record for DONJOY NEXTEP WALKER is Span Link International, LLC.
What is the Primary UDI-DI identifier for DONJOY NEXTEP WALKER?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 01220000531765.
What classification code is assigned to this device?
This device is registered under product classification code Y06120601.
Similar Classification Devices (Y06120601)
Other Devices by Span Link International, LLC
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint