eudamed_udi
Primary ID: 06941691973232
TOCO Fetal transducer (UDI 06941691973232)
Manufactured by Orantech Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for TOCO Fetal transducer - Primary ID 06941691973232
Device Regulatory Overview
The TOCO Fetal transducer (Model/Catalog Number: FTC-LK01) is a medical device manufactured by Orantech Inc.. This product is indexed under FDA Product Code / Category Classification Z12080101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- FTC-LK01
- Product Code / EMDN
- Z12080101
- Device Name
- TOCO Fetal transducer
- Database Sync Date
- 2026-08-09 17:13:38
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 TOCO Fetal transducer?
The registered manufacturer of record for TOCO Fetal transducer is Orantech Inc..
What is the Primary UDI-DI identifier for TOCO Fetal transducer?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06941691973232.
What classification code is assigned to this device?
This device is registered under product classification code Z12080101.
Similar Classification Devices (Z12080101)
Other Devices by Orantech Inc.
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