eudamed_udi
Primary ID: 08056351381086
APRIBOCCA (UDI 08056351381086)
Manufactured by TAUMEDIPLAST s.r.l.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for APRIBOCCA - Primary ID 08056351381086
Device Regulatory Overview
The APRIBOCCA (Model/Catalog Number: APRIBOCCA) is a medical device manufactured by TAUMEDIPLAST s.r.l.. This product is indexed under FDA Product Code / Category Classification R9001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- APRIBOCCA
- Product Code / EMDN
- R9001
- Device Name
- APRIBOCCA
- Database Sync Date
- 2026-08-09 16:51:26
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 APRIBOCCA?
The registered manufacturer of record for APRIBOCCA is TAUMEDIPLAST s.r.l..
What is the Primary UDI-DI identifier for APRIBOCCA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08056351381086.
What classification code is assigned to this device?
This device is registered under product classification code R9001.
Similar Classification Devices (R9001)
Other Devices by TAUMEDIPLAST s.r.l.
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