gudid
Primary ID: SES-240
Koala (UDI SES-240)
Manufactured by BOSTON SCIENTIFIC CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Koala - Primary ID SES-240
Device Regulatory Overview
The Koala (Model/Catalog Number: SES-240) is a medical device manufactured by BOSTON SCIENTIFIC CORPORATION. This product is indexed under FDA Product Code / Category Classification MNL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SES-240
- Product Code / EMDN
- MNL
- Device Name
- Cleaning Sponge plus Pure Enzymatic
- Database Sync Date
- 2026-08-09 09:12:10
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 Koala?
The registered manufacturer of record for Koala is BOSTON SCIENTIFIC CORPORATION.
What is the Primary UDI-DI identifier for Koala?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SES-240.
What classification code is assigned to this device?
This device is registered under product classification code MNL.
Similar Classification Devices (MNL)
Other Devices by BOSTON SCIENTIFIC CORPORATION
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