eudamed_udi
Primary ID: 04260181256887
TMS Active X-Wipes (UDI 04260181256887)
Manufactured by Laboratorium Dr. Deppe GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TMS Active X-Wipes - Primary ID 04260181256887
Device Regulatory Overview
The TMS Active X-Wipes (Model/Catalog Number: 601928) is a medical device manufactured by Laboratorium Dr. Deppe GmbH. This product is indexed under FDA Product Code / Category Classification D0701 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 601928
- Product Code / EMDN
- D0701
- Device Name
- Surface Disinfectant
- Database Sync Date
- 2026-08-09 16:48:40
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 TMS Active X-Wipes?
The registered manufacturer of record for TMS Active X-Wipes is Laboratorium Dr. Deppe GmbH.
What is the Primary UDI-DI identifier for TMS Active X-Wipes?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260181256887.
What classification code is assigned to this device?
This device is registered under product classification code D0701.
Similar Classification Devices (D0701)
Other Devices by Laboratorium Dr. Deppe GmbH
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