eudamed_udi
Primary ID: 06926515402938
Breitfixierpflaster (UDI 06926515402938)
Manufactured by Zhende Medical Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Breitfixierpflaster - Primary ID 06926515402938
Device Regulatory Overview
The Breitfixierpflaster (Model/Catalog Number: 138945) is a medical device manufactured by Zhende Medical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification M04010201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 138945
- Product Code / EMDN
- M04010201
- Device Name
- Medical dressing roll
- Database Sync Date
- 2026-08-09 16:29:06
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 Breitfixierpflaster?
The registered manufacturer of record for Breitfixierpflaster is Zhende Medical Co., Ltd..
What is the Primary UDI-DI identifier for Breitfixierpflaster?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06926515402938.
What classification code is assigned to this device?
This device is registered under product classification code M04010201.
Similar Classification Devices (M04010201)
Other Devices by Zhende Medical Co., Ltd.
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