gudid
Primary ID: 30655
Biogel Sensor (UDI 30655)
Manufactured by Mlnlycke Health Care AB
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Biogel Sensor - Primary ID 30655
Device Regulatory Overview
The Biogel Sensor (Model/Catalog Number: 30655) is a medical device manufactured by Mlnlycke Health Care AB. This product is indexed under FDA Product Code / Category Classification KGO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 30655
- Product Code / EMDN
- KGO
- Device Name
- Biogel Sensor 5.5 x 50 US
- Database Sync Date
- 2026-08-09 09:08:08
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 Biogel Sensor?
The registered manufacturer of record for Biogel Sensor is Mlnlycke Health Care AB.
What is the Primary UDI-DI identifier for Biogel Sensor?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 30655.
What classification code is assigned to this device?
This device is registered under product classification code KGO.
Similar Classification Devices (KGO)
Other Devices by Mlnlycke Health Care AB
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