gudid
Primary ID: 01
TT Transformer (UDI 01)
Manufactured by TT TOOTH TRANSFORMER SRL
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TT Transformer - Primary ID 01
Device Regulatory Overview
The TT Transformer (Model/Catalog Number: 01) is a medical device manufactured by TT TOOTH TRANSFORMER SRL. This product is indexed under FDA Product Code / Category Classification GEY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 01
- Product Code / EMDN
- GEY
- Device Name
- AC-powered Medical Device which allows automatic preparation of dentinal autologous material, starting from a tooth of a patient, in order to make it usable for bone regeneration, by the action of a motor that provides power to operate blades that reduce the tooth into granules.
- Database Sync Date
- 2026-08-09 09:04:30
Full Regulatory Attributes
🔒 Token Gated
{
"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 TT Transformer?
The registered manufacturer of record for TT Transformer is TT TOOTH TRANSFORMER SRL.
What is the Primary UDI-DI identifier for TT Transformer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 01.
What classification code is assigned to this device?
This device is registered under product classification code GEY.
Similar Classification Devices (GEY)
Other Devices by TT TOOTH TRANSFORMER SRL
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