eudamed_udi
Primary ID: 04260206626619
Akupunkturpflaster (UDI 04260206626619)
Manufactured by WUNDmed GmbH & Co. KG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Akupunkturpflaster - Primary ID 04260206626619
Device Regulatory Overview
The Akupunkturpflaster (Model/Catalog Number: 02-128) is a medical device manufactured by WUNDmed GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification M0599 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 02-128
- Product Code / EMDN
- M0599
- Device Name
- Kinesiologie-Tape
- Database Sync Date
- 2026-08-09 16:29:05
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 Akupunkturpflaster?
The registered manufacturer of record for Akupunkturpflaster is WUNDmed GmbH & Co. KG.
What is the Primary UDI-DI identifier for Akupunkturpflaster?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260206626619.
What classification code is assigned to this device?
This device is registered under product classification code M0599.
Similar Classification Devices (M0599)
Other Devices by WUNDmed GmbH & Co. KG
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