eudamed_udi
Primary ID: 04895237164689
Sterile Surgical Packs (UDI 04895237164689)
Manufactured by KENPAX INTERNATIONAL LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Sterile Surgical Packs - Primary ID 04895237164689
Device Regulatory Overview
The Sterile Surgical Packs (Model/Catalog Number: 70-5022-ST) is a medical device manufactured by KENPAX INTERNATIONAL LIMITED. This product is indexed under FDA Product Code / Category Classification T0202 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 70-5022-ST
- Product Code / EMDN
- T0202
- Device Name
- Sterile Surgical Packs
- Database Sync Date
- 2026-08-09 16:44:52
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 Sterile Surgical Packs?
The registered manufacturer of record for Sterile Surgical Packs is KENPAX INTERNATIONAL LIMITED.
What is the Primary UDI-DI identifier for Sterile Surgical Packs?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04895237164689.
What classification code is assigned to this device?
This device is registered under product classification code T0202.
Similar Classification Devices (T0202)
Other Devices by KENPAX INTERNATIONAL LIMITED
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