gudid
Primary ID: 100 mL
ExSept Plus (UDI 100 mL)
Manufactured by Angelini Pharma Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ExSept Plus - Primary ID 100 mL
Device Regulatory Overview
The ExSept Plus (Model/Catalog Number: 100 mL) is a medical device manufactured by Angelini Pharma Inc.. This product is indexed under FDA Product Code / Category Classification FQH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 100 mL
- Product Code / EMDN
- FQH
- Device Name
- Skin and would cleanser.
- Database Sync Date
- 2026-08-09 09:46:57
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 ExSept Plus?
The registered manufacturer of record for ExSept Plus is Angelini Pharma Inc..
What is the Primary UDI-DI identifier for ExSept Plus?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 100 mL.
What classification code is assigned to this device?
This device is registered under product classification code FQH.
Similar Classification Devices (FQH)
Other Devices by Angelini Pharma Inc.
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