gudid
Primary ID: 2-900
Kitpack (UDI 2-900)
Manufactured by NETWORK MEDICAL PRODUCTS LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Kitpack - Primary ID 2-900
Device Regulatory Overview
The Kitpack (Model/Catalog Number: 2-900) is a medical device manufactured by NETWORK MEDICAL PRODUCTS LIMITED. This product is indexed under FDA Product Code / Category Classification HOZ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 2-900
- Product Code / EMDN
- HOZ
- Device Name
- Instrument Wipe
- Database Sync Date
- 2026-08-09 09:08:11
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 Kitpack?
The registered manufacturer of record for Kitpack is NETWORK MEDICAL PRODUCTS LIMITED.
What is the Primary UDI-DI identifier for Kitpack?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2-900.
What classification code is assigned to this device?
This device is registered under product classification code HOZ.
Similar Classification Devices (HOZ)
Other Devices by NETWORK MEDICAL PRODUCTS LIMITED
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