gudid
Primary ID: CP-4201
Capette (UDI CP-4201)
Manufactured by SUNMED, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Capette - Primary ID CP-4201
Device Regulatory Overview
The Capette (Model/Catalog Number: CP-4201) is a medical device manufactured by SUNMED, LLC. This product is indexed under FDA Product Code / Category Classification JAY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CP-4201
- Product Code / EMDN
- JAY
- Device Name
- Small Capette with Small Tube Tackles
- Database Sync Date
- 2026-08-09 09:04:13
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 Capette?
The registered manufacturer of record for Capette is SUNMED, LLC.
What is the Primary UDI-DI identifier for Capette?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CP-4201.
What classification code is assigned to this device?
This device is registered under product classification code JAY.
Similar Classification Devices (JAY)
Other Devices by SUNMED, LLC
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