eudamed_udi
Primary ID: 05902643926356
Phenylboronic Acid (UDI 05902643926356)
Manufactured by BioMaxima Spółka Akcyjna
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Phenylboronic Acid - Primary ID 05902643926356
Device Regulatory Overview
The Phenylboronic Acid (Model/Catalog Number: SL 0136- 2ML) is a medical device manufactured by BioMaxima Spółka Akcyjna. This product is indexed under FDA Product Code / Category Classification W0104010104 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SL 0136- 2ML
- Product Code / EMDN
- W0104010104
- Device Name
- Horse Serum
- Database Sync Date
- 2026-08-09 17:27:11
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 Phenylboronic Acid?
The registered manufacturer of record for Phenylboronic Acid is BioMaxima Spółka Akcyjna.
What is the Primary UDI-DI identifier for Phenylboronic Acid?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05902643926356.
What classification code is assigned to this device?
This device is registered under product classification code W0104010104.
Similar Classification Devices (W0104010104)
Other Devices by BioMaxima Spółka Akcyjna
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