GUDIDData
eudamed_udi Primary ID: 04719892933339

RPS KNIT S4 BELT (UDI 04719892933339)

Manufactured by Zhangpu Ortholife Rehabilitation Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RPS KNIT S4 BELT - Primary ID 04719892933339

Device Regulatory Overview

The RPS KNIT S4 BELT (Model/Catalog Number: 251102(XL/UNI/Black)) is a medical device manufactured by Zhangpu Ortholife Rehabilitation Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Y060303 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
251102(XL/UNI/Black)
Product Code / EMDN
Y060303
Device Name
Back Brace (Pelvic Support)
Database Sync Date
2026-08-09 17:47:35

Full Regulatory Attributes

🔒 Token Gated
{
    "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 RPS KNIT S4 BELT?

The registered manufacturer of record for RPS KNIT S4 BELT is Zhangpu Ortholife Rehabilitation Co., Ltd..

What is the Primary UDI-DI identifier for RPS KNIT S4 BELT?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04719892933339.

What classification code is assigned to this device?

This device is registered under product classification code Y060303.

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