eudamed_udi
Primary ID: 05029053509525
Depend Anatomické Vložné plenky (UDI 05029053509525)
Manufactured by KIMBERLY-CLARK B.V.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Depend Anatomické Vložné plenky - Primary ID 05029053509525
Device Regulatory Overview
The Depend Anatomické Vložné plenky (Model/Catalog Number: 1995312) is a medical device manufactured by KIMBERLY-CLARK B.V.. This product is indexed under FDA Product Code / Category Classification T04010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1995312
- Product Code / EMDN
- T04010101
- Device Name
- Dep Slip Inlay 30x6 Bx
- Database Sync Date
- 2026-08-09 17:00:07
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 Depend Anatomické Vložné plenky?
The registered manufacturer of record for Depend Anatomické Vložné plenky is KIMBERLY-CLARK B.V..
What is the Primary UDI-DI identifier for Depend Anatomické Vložné plenky?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05029053509525.
What classification code is assigned to this device?
This device is registered under product classification code T04010101.
Similar Classification Devices (T04010101)
Other Devices by KIMBERLY-CLARK B.V.
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