eudamed_udi
Primary ID: 05907514602216
ACCENT-300 ALP (UDI 05907514602216)
Manufactured by PZ CORMAY Spółka Akcyjna
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ACCENT-300 ALP - Primary ID 05907514602216
Device Regulatory Overview
The ACCENT-300 ALP (Model/Catalog Number: 7-312) is a medical device manufactured by PZ CORMAY Spółka Akcyjna. This product is indexed under FDA Product Code / Category Classification W01010105 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7-312
- Product Code / EMDN
- W01010105
- Device Name
- ALP
- Database Sync Date
- 2026-08-09 16:45:50
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 ACCENT-300 ALP?
The registered manufacturer of record for ACCENT-300 ALP is PZ CORMAY Spółka Akcyjna.
What is the Primary UDI-DI identifier for ACCENT-300 ALP?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05907514602216.
What classification code is assigned to this device?
This device is registered under product classification code W01010105.
Similar Classification Devices (W01010105)
Other Devices by PZ CORMAY Spółka Akcyjna
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