Full Length Insole (UDI 04719872866572)
Manufactured by Zhangpu Ortholife Rehabilitation Co., Ltd.
Device Regulatory Overview
The Full Length Insole (Model/Catalog Number: 640001(S/UNI/White)) is a medical device manufactured by Zhangpu Ortholife Rehabilitation Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Y061203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 640001(S/UNI/White)
- Product Code / EMDN
- Y061203
- Device Name
- Insole (Orthotic insole)
- Database Sync Date
- 2026-08-09 16:28:59
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 Full Length Insole?
The registered manufacturer of record for Full Length Insole is Zhangpu Ortholife Rehabilitation Co., Ltd..
What is the Primary UDI-DI identifier for Full Length Insole?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04719872866572.
What classification code is assigned to this device?
This device is registered under product classification code Y061203.
Similar Classification Devices (Y061203)
Other Devices by Zhangpu Ortholife Rehabilitation Co., Ltd.
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