BUN-ΟΥΡΙΑ R1:4x44 R2:2x22 ml (UR8210/PPC300N) (UDI 05213003193838)
Manufactured by Biotechnological Applications Ltd
Device Regulatory Overview
The BUN-ΟΥΡΙΑ R1:4x44 R2:2x22 ml (UR8210/PPC300N) (Model/Catalog Number: 002518) is a medical device manufactured by Biotechnological Applications Ltd. This product is indexed under FDA Product Code / Category Classification W01010204 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 002518
- Product Code / EMDN
- W01010204
- Device Name
- BUN-ΟΥΡΙΑ R1:4x44, R2:2x22 ml (UR8210/PPC300N)
- Database Sync Date
- 2026-08-09 16:48:40
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of BUN-ΟΥΡΙΑ R1:4x44 R2:2x22 ml (UR8210/PPC300N)?
The registered manufacturer of record for BUN-ΟΥΡΙΑ R1:4x44 R2:2x22 ml (UR8210/PPC300N) is Biotechnological Applications Ltd.
What is the Primary UDI-DI identifier for BUN-ΟΥΡΙΑ R1:4x44 R2:2x22 ml (UR8210/PPC300N)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05213003193838.
What classification code is assigned to this device?
This device is registered under product classification code W01010204.
Similar Classification Devices (W01010204)
Other Devices by Biotechnological Applications Ltd
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint