eudamed_udi
Primary ID: 04260181256382
peseptan e XXL Bio Wipes (UDI 04260181256382)
Manufactured by Laboratorium Dr. Deppe GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for peseptan e XXL Bio Wipes - Primary ID 04260181256382
Device Regulatory Overview
The peseptan e XXL Bio Wipes (Model/Catalog Number: 600874) 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
- 600874
- Product Code / EMDN
- D0701
- Device Name
- Surface Disinfectant
- Database Sync Date
- 2026-08-09 16:50:43
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 peseptan e XXL Bio Wipes?
The registered manufacturer of record for peseptan e XXL Bio Wipes is Laboratorium Dr. Deppe GmbH.
What is the Primary UDI-DI identifier for peseptan e XXL Bio Wipes?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260181256382.
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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint