Unspecified Brand (UDI 06978248701437)
Manufactured by FOSHAN NANHAI DEYANG DEVELOPMENT REHABILITATION EQUIPMENT CO., LTD
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: DY-963L) is a medical device manufactured by FOSHAN NANHAI DEYANG DEVELOPMENT REHABILITATION EQUIPMENT CO., LTD. This product is indexed under FDA Product Code / Category Classification Y120606 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DY-963L
- Product Code / EMDN
- Y120606
- Device Name
- Walking Frame
- Database Sync Date
- 2026-08-09 16:28:52
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is FOSHAN NANHAI DEYANG DEVELOPMENT REHABILITATION EQUIPMENT CO., LTD.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06978248701437.
What classification code is assigned to this device?
This device is registered under product classification code Y120606.
Similar Classification Devices (Y120606)
Other Devices by FOSHAN NANHAI DEYANG DEVELOPMENT REHABILITATION EQUIPMENT CO., LTD
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint