eudamed_udi
Primary ID: 04067746000714
Connector (UDI 04067746000714)
Manufactured by HMT Medizintechnik GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Connector - Primary ID 04067746000714
Device Regulatory Overview
The Connector (Model/Catalog Number: K3320) is a medical device manufactured by HMT Medizintechnik GmbH. This product is indexed under FDA Product Code / Category Classification A070199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- K3320
- Product Code / EMDN
- A070199
- Device Name
- HMT CONNECTOR
- Database Sync Date
- 2026-08-09 16:46:14
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 Connector?
The registered manufacturer of record for Connector is HMT Medizintechnik GmbH.
What is the Primary UDI-DI identifier for Connector?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04067746000714.
What classification code is assigned to this device?
This device is registered under product classification code A070199.
Similar Classification Devices (A070199)
Other Devices by HMT Medizintechnik GmbH
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