gudid
Primary ID: Breast Interface
Delphinus Sequr (UDI Breast Interface)
Manufactured by PARKER LABORATORIES INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Delphinus Sequr - Primary ID Breast Interface
Device Regulatory Overview
The Delphinus Sequr (Model/Catalog Number: Breast Interface) is a medical device manufactured by PARKER LABORATORIES INC. This product is indexed under FDA Product Code / Category Classification IYO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Breast Interface
- Product Code / EMDN
- IYO
- Device Name
- Delphinus Sequr Breast Interface - GEL PAD
- Database Sync Date
- 2026-08-09 09:49:29
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 Delphinus Sequr?
The registered manufacturer of record for Delphinus Sequr is PARKER LABORATORIES INC.
What is the Primary UDI-DI identifier for Delphinus Sequr?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Breast Interface.
What classification code is assigned to this device?
This device is registered under product classification code IYO.
Similar Classification Devices (IYO)
Other Devices by PARKER LABORATORIES INC
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