gudid
Primary ID: Pad
Kotex (UDI Pad)
Manufactured by Kimberly Clark Costa Rica Ltda
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kotex - Primary ID Pad
Device Regulatory Overview
The Kotex (Model/Catalog Number: Pad) is a medical device manufactured by Kimberly Clark Costa Rica Ltda. This product is indexed under FDA Product Code / Category Classification HHD within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Pad
- Product Code / EMDN
- HHD
- Device Name
- TOA FEM KOT NOCT TELA C/A 16X8 PR
- Database Sync Date
- 2026-08-09 09:07:23
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 Kotex?
The registered manufacturer of record for Kotex is Kimberly Clark Costa Rica Ltda.
What is the Primary UDI-DI identifier for Kotex?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Pad.
What classification code is assigned to this device?
This device is registered under product classification code HHD.
Similar Classification Devices (HHD)
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