gudid
Primary ID: CEK-9105
Compliance EndoKit (UDI CEK-9105)
Manufactured by BOSTON SCIENTIFIC CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Compliance EndoKit - Primary ID CEK-9105
Device Regulatory Overview
The Compliance EndoKit (Model/Catalog Number: CEK-9105) 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
- CEK-9105
- Product Code / EMDN
- MNL
- Device Name
- Compliance EndoKit
- 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 Compliance EndoKit?
The registered manufacturer of record for Compliance EndoKit is BOSTON SCIENTIFIC CORPORATION.
What is the Primary UDI-DI identifier for Compliance EndoKit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CEK-9105.
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
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint