ViVi® TOGA SIZE XL_XXL (UDI 09009607802209)
Manufactured by THI Total Healthcare Innovation GmbH
Device Regulatory Overview
The ViVi® TOGA SIZE XL_XXL (Model/Catalog Number: 80220) is a medical device manufactured by THI Total Healthcare Innovation GmbH. This product is indexed under FDA Product Code / Category Classification T020401 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 80220
- Product Code / EMDN
- T020401
- Device Name
- ViVi® GOWNS 80XXX
- Database Sync Date
- 2026-08-09 18:27:26
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 ViVi® TOGA SIZE XL_XXL?
The registered manufacturer of record for ViVi® TOGA SIZE XL_XXL is THI Total Healthcare Innovation GmbH.
What is the Primary UDI-DI identifier for ViVi® TOGA SIZE XL_XXL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 09009607802209.
What classification code is assigned to this device?
This device is registered under product classification code T020401.
Similar Classification Devices (T020401)
Other Devices by THI Total Healthcare Innovation GmbH
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