gudid
Primary ID: AC+203
MedicaPure (UDI AC+203)
Manufactured by DIMESOL USA, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MedicaPure - Primary ID AC+203
Device Regulatory Overview
The MedicaPure (Model/Catalog Number: AC+203) is a medical device manufactured by DIMESOL USA, LLC. This product is indexed under FDA Product Code / Category Classification KPO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AC+203
- Product Code / EMDN
- KPO
- Device Name
- Liquid Acid Concentrate
- Database Sync Date
- 2026-08-09 09:31:19
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 MedicaPure?
The registered manufacturer of record for MedicaPure is DIMESOL USA, LLC.
What is the Primary UDI-DI identifier for MedicaPure?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is AC+203.
What classification code is assigned to this device?
This device is registered under product classification code KPO.
Similar Classification Devices (KPO)
Other Devices by DIMESOL USA, LLC
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