GOT LIQUID R1:4x44, R2:2x22 ml (UR8210/PPC300N) (UDI 05213003193906)
Manufactured by Biotechnological Applications Ltd
Device Regulatory Overview
The GOT LIQUID R1:4x44, R2:2x22 ml (UR8210/PPC300N) (Model/Catalog Number: 002529) is a medical device manufactured by Biotechnological Applications Ltd. This product is indexed under FDA Product Code / Category Classification W01010110 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 002529
- Product Code / EMDN
- W01010110
- Device Name
- GOT LIQUID R1:4x44, R2:2x22 ml (UR8210/PPC300N)
- Database Sync Date
- 2026-08-09 17:29:00
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 GOT LIQUID R1:4x44, R2:2x22 ml (UR8210/PPC300N)?
The registered manufacturer of record for GOT LIQUID R1:4x44, R2:2x22 ml (UR8210/PPC300N) is Biotechnological Applications Ltd.
What is the Primary UDI-DI identifier for GOT LIQUID R1:4x44, R2:2x22 ml (UR8210/PPC300N)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05213003193906.
What classification code is assigned to this device?
This device is registered under product classification code W01010110.
Similar Classification Devices (W01010110)
Other Devices by Biotechnological Applications Ltd
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