gudid
Primary ID: MD35/CW1A/TL400 Doppler Barrel
Hokanson (UDI MD35/CW1A/TL400 Doppler Barrel)
Manufactured by D.E.HOKANSON, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Hokanson - Primary ID MD35/CW1A/TL400 Doppler Barrel
Device Regulatory Overview
The Hokanson (Model/Catalog Number: MD35/CW1A/TL400 Doppler Barrel) is a medical device manufactured by D.E.HOKANSON, INC.. This product is indexed under FDA Product Code / Category Classification DSB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MD35/CW1A/TL400 Doppler Barrel
- Product Code / EMDN
- DSB
- Device Name
- DOPPLER PROBE BARREL - A Doppler sensor only.
- Database Sync Date
- 2026-08-09 09:31:22
Full Regulatory Attributes
🔒 Token Gated
{
"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 Hokanson?
The registered manufacturer of record for Hokanson is D.E.HOKANSON, INC..
What is the Primary UDI-DI identifier for Hokanson?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is MD35/CW1A/TL400 Doppler Barrel.
What classification code is assigned to this device?
This device is registered under product classification code DSB.
Similar Classification Devices (DSB)
Other Devices by D.E.HOKANSON, INC.
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