eudamed_udi
Primary ID: 05907514674138
A-400 COMPLEMENT C4 (UDI 05907514674138)
Manufactured by PZ CORMAY Spółka Akcyjna
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for A-400 COMPLEMENT C4 - Primary ID 05907514674138
Device Regulatory Overview
The A-400 COMPLEMENT C4 (Model/Catalog Number: 7-413) is a medical device manufactured by PZ CORMAY Spółka Akcyjna. This product is indexed under FDA Product Code / Category Classification W0102010205 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7-413
- Product Code / EMDN
- W0102010205
- Device Name
- COMPLEMENT C4
- Database Sync Date
- 2026-08-09 18:12:31
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 A-400 COMPLEMENT C4?
The registered manufacturer of record for A-400 COMPLEMENT C4 is PZ CORMAY Spółka Akcyjna.
What is the Primary UDI-DI identifier for A-400 COMPLEMENT C4?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05907514674138.
What classification code is assigned to this device?
This device is registered under product classification code W0102010205.
Similar Classification Devices (W0102010205)
Other Devices by PZ CORMAY Spółka Akcyjna
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