GUDIDData
eudamed_udi Primary ID: 06975371492591

ROLLATOR (UDI 06975371492591)

Manufactured by Foshan Kaiyang Medical Equipment Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ROLLATOR - Primary ID 06975371492591

Device Regulatory Overview

The ROLLATOR (Model/Catalog Number: KY9141L BLUE) is a medical device manufactured by Foshan Kaiyang Medical Equipment Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Y120612 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
KY9141L BLUE
Product Code / EMDN
Y120612
Device Name
WALKER
Database Sync Date
2026-08-09 16:44:47

Full Regulatory Attributes

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{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of ROLLATOR?

The registered manufacturer of record for ROLLATOR is Foshan Kaiyang Medical Equipment Co., Ltd..

What is the Primary UDI-DI identifier for ROLLATOR?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975371492591.

What classification code is assigned to this device?

This device is registered under product classification code Y120612.

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