eudamed_udi
Primary ID: 08053470800122
Unspecified Brand (UDI 08053470800122)
Manufactured by Gammadis Farmaceutici Srl
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 08053470800122
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: 160110 - 160111 - 160112) is a medical device manufactured by Gammadis Farmaceutici Srl. This product is indexed under FDA Product Code / Category Classification T01010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 160110 - 160111 - 160112
- Product Code / EMDN
- T01010102
- Device Name
- Guanti in Lattice senza polvere
- Database Sync Date
- 2026-08-09 16:29:13
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Gammadis Farmaceutici Srl.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08053470800122.
What classification code is assigned to this device?
This device is registered under product classification code T01010102.
Similar Classification Devices (T01010102)
Other Devices by Gammadis Farmaceutici Srl
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