eudamed_udi
Primary ID: 08055727371171
ACETABULÁRNÍ FRÉZA D56 mm HC (UDI 08055727371171)
Manufactured by HPF S.R.L.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ACETABULÁRNÍ FRÉZA D56 mm HC - Primary ID 08055727371171
Device Regulatory Overview
The ACETABULÁRNÍ FRÉZA D56 mm HC (Model/Catalog Number: 01.30.10.3256) is a medical device manufactured by HPF S.R.L.. This product is indexed under FDA Product Code / Category Classification L091102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 01.30.10.3256
- Product Code / EMDN
- L091102
- Device Name
- Full cross – HPF – half cross acetabular reamer
- Database Sync Date
- 2026-08-09 16:29:06
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 ACETABULÁRNÍ FRÉZA D56 mm HC?
The registered manufacturer of record for ACETABULÁRNÍ FRÉZA D56 mm HC is HPF S.R.L..
What is the Primary UDI-DI identifier for ACETABULÁRNÍ FRÉZA D56 mm HC?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08055727371171.
What classification code is assigned to this device?
This device is registered under product classification code L091102.
Similar Classification Devices (L091102)
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