gudid
Primary ID: 10-4032-10NKS
INSTRUSAFE (UDI 10-4032-10NKS)
Manufactured by SHIPPERT MEDICAL TECHNOLOGIES, INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for INSTRUSAFE - Primary ID 10-4032-10NKS
Device Regulatory Overview
The INSTRUSAFE (Model/Catalog Number: 10-4032-10NKS) is a medical device manufactured by SHIPPERT MEDICAL TECHNOLOGIES, INC. This product is indexed under FDA Product Code / Category Classification EPP within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10-4032-10NKS
- Product Code / EMDN
- EPP
- Device Name
- Database Sync Date
- 2026-08-09 09:22:09
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 INSTRUSAFE?
The registered manufacturer of record for INSTRUSAFE is SHIPPERT MEDICAL TECHNOLOGIES, INC.
What is the Primary UDI-DI identifier for INSTRUSAFE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10-4032-10NKS.
What classification code is assigned to this device?
This device is registered under product classification code EPP.
Similar Classification Devices (EPP)
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