gudid
Primary ID: Z530M2201
ZD (UDI Z530M2201)
Manufactured by Xuchang Zhende Surgical Dressing Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ZD - Primary ID Z530M2201
Device Regulatory Overview
The ZD (Model/Catalog Number: Z530M2201) is a medical device manufactured by Xuchang Zhende Surgical Dressing Co., Ltd.. This product is indexed under FDA Product Code / Category Classification LKB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Z530M2201
- Product Code / EMDN
- LKB
- Device Name
- Alcohol prep pad 1.1875 x 1.35 in
- Database Sync Date
- 2026-08-09 09:06:41
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 ZD?
The registered manufacturer of record for ZD is Xuchang Zhende Surgical Dressing Co., Ltd..
What is the Primary UDI-DI identifier for ZD?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Z530M2201.
What classification code is assigned to this device?
This device is registered under product classification code LKB.
Similar Classification Devices (LKB)
Other Devices by Xuchang Zhende Surgical Dressing Co., Ltd.
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