eudamed_udi
Primary ID: 09556807342108
esme (UDI 09556807342108)
Manufactured by Richter Rubber Technology Sdn Bhd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for esme - Primary ID 09556807342108
Device Regulatory Overview
The esme (Model/Catalog Number: QA-224) is a medical device manufactured by Richter Rubber Technology Sdn Bhd. This product is indexed under FDA Product Code / Category Classification U110101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- QA-224
- Product Code / EMDN
- U110101
- Device Name
- Non-Medicated Natural Latex Condoms
- Database Sync Date
- 2026-08-09 16:28:45
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 esme?
The registered manufacturer of record for esme is Richter Rubber Technology Sdn Bhd.
What is the Primary UDI-DI identifier for esme?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 09556807342108.
What classification code is assigned to this device?
This device is registered under product classification code U110101.
Similar Classification Devices (U110101)
Other Devices by Richter Rubber Technology Sdn Bhd
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