eudamed_udi
Primary ID: 06976144642281
Manual wheelchair (UDI 06976144642281)
Manufactured by NINGBO KS MEDICAL TECH CO.,LTD
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Manual wheelchair - Primary ID 06976144642281
Device Regulatory Overview
The Manual wheelchair (Model/Catalog Number: KSM202) is a medical device manufactured by NINGBO KS MEDICAL TECH CO.,LTD. This product is indexed under FDA Product Code / Category Classification Y122103 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- KSM202
- Product Code / EMDN
- Y122103
- Device Name
- Manual Wheelchair
- Database Sync Date
- 2026-08-09 16:29:10
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Manual wheelchair?
The registered manufacturer of record for Manual wheelchair is NINGBO KS MEDICAL TECH CO.,LTD.
What is the Primary UDI-DI identifier for Manual wheelchair?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06976144642281.
What classification code is assigned to this device?
This device is registered under product classification code Y122103.
Similar Classification Devices (Y122103)
Other Devices by NINGBO KS MEDICAL TECH CO.,LTD
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