gudid
Primary ID: 1003-00-101
KINCISE (UDI 1003-00-101)
Manufactured by Synthes GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for KINCISE - Primary ID 1003-00-101
Device Regulatory Overview
The KINCISE (Model/Catalog Number: 1003-00-101) is a medical device manufactured by Synthes GmbH. This product is indexed under FDA Product Code / Category Classification GEY within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1003-00-101
- Product Code / EMDN
- GEY
- Device Name
- KINCISE 4-PORT BATTERY CHARGER
- Database Sync Date
- 2026-08-09 09:21:09
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 KINCISE?
The registered manufacturer of record for KINCISE is Synthes GmbH.
What is the Primary UDI-DI identifier for KINCISE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 1003-00-101.
What classification code is assigned to this device?
This device is registered under product classification code GEY.
Similar Classification Devices (GEY)
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