Unspecified Brand (UDI 06941571852107)
Manufactured by Ameritech Diagnostic Reagent (Jiaxing) Co., Ltd.
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: R52-112) is a medical device manufactured by Ameritech Diagnostic Reagent (Jiaxing) Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W0102160599 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- R52-112
- Product Code / EMDN
- W0102160599
- Device Name
- Ketamine Test
- Database Sync Date
- 2026-08-09 16:30:17
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Ameritech Diagnostic Reagent (Jiaxing) Co., Ltd..
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06941571852107.
What classification code is assigned to this device?
This device is registered under product classification code W0102160599.
Similar Classification Devices (W0102160599)
Other Devices by Ameritech Diagnostic Reagent (Jiaxing) Co., Ltd.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint