eudamed_udi
Primary ID: 08057968715035
PRØVEKOP D37 mm (UDI 08057968715035)
Manufactured by HPF S.R.L.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PRØVEKOP D37 mm - Primary ID 08057968715035
Device Regulatory Overview
The PRØVEKOP D37 mm (Model/Catalog Number: H0030150309) is a medical device manufactured by HPF S.R.L.. This product is indexed under FDA Product Code / Category Classification V06010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- H0030150309
- Product Code / EMDN
- V06010101
- Device Name
- Trial cup
- Database Sync Date
- 2026-08-09 16:49:43
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 PRØVEKOP D37 mm?
The registered manufacturer of record for PRØVEKOP D37 mm is HPF S.R.L..
What is the Primary UDI-DI identifier for PRØVEKOP D37 mm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08057968715035.
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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