eudamed_udi
Primary ID: 06937845503080
TK (UDI 06937845503080)
Manufactured by Guangzhou T.K Medical instrument Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TK - Primary ID 06937845503080
Device Regulatory Overview
The TK (Model/Catalog Number: HSD-130/D) is a medical device manufactured by Guangzhou T.K Medical instrument Co., Ltd.. This product is indexed under FDA Product Code / Category Classification A090101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HSD-130/D
- Product Code / EMDN
- A090101
- Device Name
- Retriever Bags
- Database Sync Date
- 2026-08-09 16:30:06
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 TK?
The registered manufacturer of record for TK is Guangzhou T.K Medical instrument Co., Ltd..
What is the Primary UDI-DI identifier for TK?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06937845503080.
What classification code is assigned to this device?
This device is registered under product classification code A090101.
Similar Classification Devices (A090101)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint