BGA LAB-AGAR™ acc. to ISO 6579 (UDI 05902643903968)
Manufactured by BioMaxima Spółka Akcyjna
Device Regulatory Overview
The BGA LAB-AGAR™ acc. to ISO 6579 (Model/Catalog Number: PS 98- 500) 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 98- 500
- Product Code / EMDN
- W0104010101
- Device Name
- BGA LAB-AGAR™ acc. to ISO 6579
- Database Sync Date
- 2026-08-09 16:30:04
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 BGA LAB-AGAR™ acc. to ISO 6579?
The registered manufacturer of record for BGA LAB-AGAR™ acc. to ISO 6579 is BioMaxima Spółka Akcyjna.
What is the Primary UDI-DI identifier for BGA LAB-AGAR™ acc. to ISO 6579?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05902643903968.
What classification code is assigned to this device?
This device is registered under product classification code W0104010101.
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