gudid
Primary ID: TYC2020
Themy (UDI TYC2020)
Manufactured by M.D.L. S.R.L.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Themy - Primary ID TYC2020
Device Regulatory Overview
The Themy (Model/Catalog Number: TYC2020) is a medical device manufactured by M.D.L. S.R.L.. This product is indexed under FDA Product Code / Category Classification FCG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TYC2020
- Product Code / EMDN
- FCG
- Device Name
- THEMY AUTOMATIC NEEDLE 20Gx200mmNOTCH 20mm, WITH COAXIAL NEEDLEFOR SOFT TISSUE BIOPSY
- Database Sync Date
- 2026-08-09 09:04:30
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 Themy?
The registered manufacturer of record for Themy is M.D.L. S.R.L..
What is the Primary UDI-DI identifier for Themy?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is TYC2020.
What classification code is assigned to this device?
This device is registered under product classification code FCG.
Similar Classification Devices (FCG)
Other Devices by M.D.L. S.R.L.
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