Heka Plast transparante eilandpleisters met border (UDI 06922096406204)
Manufactured by Jiangsu Nanfang Medical Co., Ltd.
Device Regulatory Overview
The Heka Plast transparante eilandpleisters met border (Model/Catalog Number: /) is a medical device manufactured by Jiangsu Nanfang Medical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification M04010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- /
- Product Code / EMDN
- M04010102
- Device Name
- eilandpleister
- Database Sync Date
- 2026-08-09 16:29:11
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 Heka Plast transparante eilandpleisters met border?
The registered manufacturer of record for Heka Plast transparante eilandpleisters met border is Jiangsu Nanfang Medical Co., Ltd..
What is the Primary UDI-DI identifier for Heka Plast transparante eilandpleisters met border?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06922096406204.
What classification code is assigned to this device?
This device is registered under product classification code M04010102.
Similar Classification Devices (M04010102)
Other Devices by Jiangsu Nanfang Medical Co., Ltd.
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