eudamed_udi
Primary ID: 06975678806053
PAX (UDI 06975678806053)
Manufactured by Shanghai PAX Medical Instrument Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PAX - Primary ID 06975678806053
Device Regulatory Overview
The PAX (Model/Catalog Number: DS-ⅡE) is a medical device manufactured by Shanghai PAX Medical Instrument Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z12011202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DS-ⅡE
- Product Code / EMDN
- Z12011202
- Device Name
- Operating Table
- Database Sync Date
- 2026-08-09 16:30:27
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 PAX?
The registered manufacturer of record for PAX is Shanghai PAX Medical Instrument Co., Ltd..
What is the Primary UDI-DI identifier for PAX?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975678806053.
What classification code is assigned to this device?
This device is registered under product classification code Z12011202.
Similar Classification Devices (Z12011202)
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