eudamed_udi
Primary ID: 08033837938040
C-22 PLUS (UDI 08033837938040)
Manufactured by CEFLA s.c.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for C-22 PLUS - Primary ID 08033837938040
Device Regulatory Overview
The C-22 PLUS (Model/Catalog Number: 7AC21xxx) is a medical device manufactured by CEFLA s.c.. This product is indexed under FDA Product Code / Category Classification Z12011305 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 7AC21xxx
- Product Code / EMDN
- Z12011305
- Device Name
- Steam sterilizing units
- Database Sync Date
- 2026-08-09 16:45:58
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 C-22 PLUS?
The registered manufacturer of record for C-22 PLUS is CEFLA s.c..
What is the Primary UDI-DI identifier for C-22 PLUS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08033837938040.
What classification code is assigned to this device?
This device is registered under product classification code Z12011305.
Similar Classification Devices (Z12011305)
Other Devices by CEFLA s.c.
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