eudamed_udi
Primary ID: 06922096405801
eilandpleister (UDI 06922096405801)
Manufactured by Jiangsu Nanfang Medical Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for eilandpleister - Primary ID 06922096405801
Device Regulatory Overview
The eilandpleister (Model/Catalog Number: /) is a medical device manufactured by Jiangsu Nanfang Medical Co., Ltd.. This product is indexed under FDA Product Code / Category Classification M04010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- /
- Product Code / EMDN
- M04010101
- Device Name
- eilandpleister
- Database Sync Date
- 2026-08-09 16:48:57
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of eilandpleister?
The registered manufacturer of record for eilandpleister is Jiangsu Nanfang Medical Co., Ltd..
What is the Primary UDI-DI identifier for eilandpleister?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06922096405801.
What classification code is assigned to this device?
This device is registered under product classification code M04010101.
Similar Classification Devices (M04010101)
Other Devices by Jiangsu Nanfang Medical Co., Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint