eudamed_udi
Primary ID: 08050323059355
ACORN: Trial Cup Ø 52mm (UDI 08050323059355)
Manufactured by Permedica S.p.A
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ACORN: Trial Cup Ø 52mm - Primary ID 08050323059355
Device Regulatory Overview
The ACORN: Trial Cup Ø 52mm (Model/Catalog Number: S38552) is a medical device manufactured by Permedica S.p.A. This product is indexed under FDA Product Code / Category Classification V06010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- S38552
- Product Code / EMDN
- V06010101
- Device Name
- Trial Component
- Database Sync Date
- 2026-08-09 16:29:53
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 ACORN: Trial Cup Ø 52mm?
The registered manufacturer of record for ACORN: Trial Cup Ø 52mm is Permedica S.p.A.
What is the Primary UDI-DI identifier for ACORN: Trial Cup Ø 52mm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08050323059355.
What classification code is assigned to this device?
This device is registered under product classification code V06010101.
Similar Classification Devices (V06010101)
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