gudid
Primary ID: 01
Kit accessori monouso 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 Kit accessori monouso TT Transformer - Primary ID 01
Device Regulatory Overview
The Kit accessori monouso 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
- Single use kit to be exclusively used with "TT Transformer" medical device to allow its operation.
- 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
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Kit accessori monouso TT Transformer?
The registered manufacturer of record for Kit accessori monouso TT Transformer is TT TOOTH TRANSFORMER SRL.
What is the Primary UDI-DI identifier for Kit accessori monouso 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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint