gudid
Primary ID: 11344
SonoTT Vascular Probe (UDI 11344)
Manufactured by em-tec GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SonoTT Vascular Probe - Primary ID 11344
Device Regulatory Overview
The SonoTT Vascular Probe (Model/Catalog Number: 11344) is a medical device manufactured by em-tec GmbH. This product is indexed under FDA Product Code / Category Classification DPW within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 11344
- Product Code / EMDN
- DPW
- Device Name
- High quality workmanship Ultrasonic Flow Probes for the measurement ofblood flow in vessels and grafts. The probes are showing excellent accuracyand stability. Calibration data are stored in the probe.The probes can be manually and automatically cleaned and disinfected andsterilized with steam, ethylene oxide (EtO), low temperature steam and form -aldehyde sterilisation (LTSF) and low temperature plasma (LTP). We supportup to 50 sterilisation cycles
- Database Sync Date
- 2026-08-09 09:11:43
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 SonoTT Vascular Probe?
The registered manufacturer of record for SonoTT Vascular Probe is em-tec GmbH.
What is the Primary UDI-DI identifier for SonoTT Vascular Probe?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 11344.
What classification code is assigned to this device?
This device is registered under product classification code DPW.
Similar Classification Devices (DPW)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint