gudid
Primary ID: 11942
SonoTT Vascular Probe (UDI 11942)
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 11942
Device Regulatory Overview
The SonoTT Vascular Probe (Model/Catalog Number: 11942) 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
- 11942
- Product Code / EMDN
- DPW
- Device Name
- SonoTT Vascular Probe: The SonoTT Vascular Probes for measuringflow in blood vessels are available in different sizes forvessel diameters of 1.5 to 10 mm (more sizes on request).The probes can be sterilised up to 50 times using all establishedsterilisation methods (steam, EO, LTP, Formaldehyde).Automatic washing machines can be used to clean the probes.
- 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 11942.
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