One Step Multi-Drug Screen Test Key Cup (Urine) (UDI D-GBDOAA-1X6ZM)
Manufactured by Zhejiang Orient Gene Biotech Co., Ltd
Device Regulatory Overview
The One Step Multi-Drug Screen Test Key Cup (Urine) (Model/Catalog Number: GBDOAA-1X6) is a medical device manufactured by Zhejiang Orient Gene Biotech Co., Ltd. This product is indexed under FDA Product Code / Category Classification W0102090199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- GBDOAA-1X6
- Product Code / EMDN
- W0102090199
- Device Name
- One Step Multi-Drug Screen Test Key Cup (Urine)
- Database Sync Date
- 2026-08-09 16:28:53
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 One Step Multi-Drug Screen Test Key Cup (Urine)?
The registered manufacturer of record for One Step Multi-Drug Screen Test Key Cup (Urine) is Zhejiang Orient Gene Biotech Co., Ltd.
What is the Primary UDI-DI identifier for One Step Multi-Drug Screen Test Key Cup (Urine)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-GBDOAA-1X6ZM.
What classification code is assigned to this device?
This device is registered under product classification code W0102090199.
Similar Classification Devices (W0102090199)
Other Devices by Zhejiang Orient Gene Biotech Co., Ltd
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint