gudid
Primary ID: J4499
Janach (UDI J4499)
Manufactured by NETWORK MEDICAL PRODUCTS LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Janach - Primary ID J4499
Device Regulatory Overview
The Janach (Model/Catalog Number: J4499) 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
- J4499
- Product Code / EMDN
- HOZ
- Device Name
- J4499 Janach PVA LASIK Eye Drain 20 Pouches per Carton Sterile
- 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 Janach?
The registered manufacturer of record for Janach is NETWORK MEDICAL PRODUCTS LIMITED.
What is the Primary UDI-DI identifier for Janach?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is J4499.
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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