eudamed_udi
Primary ID: 05902643985117
Cetrimide LAB-AGAR™ (UDI 05902643985117)
Manufactured by BioMaxima Spółka Akcyjna
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Cetrimide LAB-AGAR™ - Primary ID 05902643985117
Device Regulatory Overview
The Cetrimide LAB-AGAR™ (Model/Catalog Number: PS 49- 250) is a medical device manufactured by BioMaxima Spółka Akcyjna. This product is indexed under FDA Product Code / Category Classification W0104010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PS 49- 250
- Product Code / EMDN
- W0104010101
- Device Name
- Cetrimide LAB-AGAR™
- Database Sync Date
- 2026-08-09 16:28:56
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 Cetrimide LAB-AGAR™?
The registered manufacturer of record for Cetrimide LAB-AGAR™ is BioMaxima Spółka Akcyjna.
What is the Primary UDI-DI identifier for Cetrimide LAB-AGAR™?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05902643985117.
What classification code is assigned to this device?
This device is registered under product classification code W0104010101.
Similar Classification Devices (W0104010101)
Other Devices by BioMaxima Spółka Akcyjna
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