AUSONIA (UDI 08001090125408)
Manufactured by Procter & Gamble Technical Centres Limited
Device Regulatory Overview
The AUSONIA (Model/Catalog Number: 80818537) is a medical device manufactured by Procter & Gamble Technical Centres Limited. This product is indexed under FDA Product Code / Category Classification T04010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 80818537
- Product Code / EMDN
- T04010102
- Device Name
- Always
- Database Sync Date
- 2026-08-09 16:46:32
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 AUSONIA?
The registered manufacturer of record for AUSONIA is Procter & Gamble Technical Centres Limited.
What is the Primary UDI-DI identifier for AUSONIA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08001090125408.
What classification code is assigned to this device?
This device is registered under product classification code T04010102.
Similar Classification Devices (T04010102)
Other Devices by Procter & Gamble Technical Centres Limited
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