ß-Ketone Control Solution L2 (UDI 04713106024431)
Manufactured by TaiDoc Technology Corporation
Device Regulatory Overview
The ß-Ketone Control Solution L2 (Model/Catalog Number: TD-4915) is a medical device manufactured by TaiDoc Technology Corporation. This product is indexed under FDA Product Code / Category Classification W0101050205 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TD-4915
- Product Code / EMDN
- W0101050205
- Device Name
- ß-Ketone control solution
- Database Sync Date
- 2026-08-09 16:48:01
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 ß-Ketone Control Solution L2?
The registered manufacturer of record for ß-Ketone Control Solution L2 is TaiDoc Technology Corporation.
What is the Primary UDI-DI identifier for ß-Ketone Control Solution L2?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04713106024431.
What classification code is assigned to this device?
This device is registered under product classification code W0101050205.
Similar Classification Devices (W0101050205)
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