gudid
Primary ID: SLT-395-10
EndoGlide+ (UDI SLT-395-10)
Manufactured by Jianerkang Medical Co., Ltd
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EndoGlide+ - Primary ID SLT-395-10
Device Regulatory Overview
The EndoGlide+ (Model/Catalog Number: SLT-395-10) is a medical device manufactured by Jianerkang Medical Co., Ltd. This product is indexed under FDA Product Code / Category Classification KMJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SLT-395-10
- Product Code / EMDN
- KMJ
- Device Name
- Database Sync Date
- 2026-08-09 09:22:49
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 EndoGlide+?
The registered manufacturer of record for EndoGlide+ is Jianerkang Medical Co., Ltd.
What is the Primary UDI-DI identifier for EndoGlide+?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SLT-395-10.
What classification code is assigned to this device?
This device is registered under product classification code KMJ.
Similar Classification Devices (KMJ)
Other Devices by Jianerkang Medical Co., Ltd
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