CUSTOM LIQUID THERAPEUTIC DRUG CONTROL - LEVEL 3 (UDI 05055273217339)
Manufactured by Randox Laboratories Limited
Device Regulatory Overview
The CUSTOM LIQUID THERAPEUTIC DRUG CONTROL - LEVEL 3 (Model/Catalog Number: HD3147) is a medical device manufactured by Randox Laboratories Limited. This product is indexed under FDA Product Code / Category Classification W0102152001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HD3147
- Product Code / EMDN
- W0102152001
- Device Name
- CUSTOM LIQUID THERAPEUTIC DRUG CONTROL
- Database Sync Date
- 2026-08-09 18:51:11
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 CUSTOM LIQUID THERAPEUTIC DRUG CONTROL - LEVEL 3?
The registered manufacturer of record for CUSTOM LIQUID THERAPEUTIC DRUG CONTROL - LEVEL 3 is Randox Laboratories Limited.
What is the Primary UDI-DI identifier for CUSTOM LIQUID THERAPEUTIC DRUG CONTROL - LEVEL 3?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05055273217339.
What classification code is assigned to this device?
This device is registered under product classification code W0102152001.
Similar Classification Devices (W0102152001)
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