eudamed_udi
Primary ID: +D7701555563
PRAMA (UDI +D7701555563)
Manufactured by SWEDEN & MARTINA S.P.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PRAMA - Primary ID +D7701555563
Device Regulatory Overview
The PRAMA (Model/Catalog Number: LA-ZT-425-180) is a medical device manufactured by SWEDEN & MARTINA S.P.A.. This product is indexed under FDA Product Code / Category Classification P01020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LA-ZT-425-180
- Product Code / EMDN
- P01020101
- Device Name
- DENTAL IMPLANT
- Database Sync Date
- 2026-08-09 16:28:59
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 PRAMA?
The registered manufacturer of record for PRAMA is SWEDEN & MARTINA S.P.A..
What is the Primary UDI-DI identifier for PRAMA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is +D7701555563.
What classification code is assigned to this device?
This device is registered under product classification code P01020101.
Similar Classification Devices (P01020101)
Other Devices by SWEDEN & MARTINA S.P.A.
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