eudamed_udi
Primary ID: 74895237130645
Operation Room Towel (UDI 74895237130645)
Manufactured by KENPAX INTERNATIONAL LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Operation Room Towel - Primary ID 74895237130645
Device Regulatory Overview
The Operation Room Towel (Model/Catalog Number: OR-1727-WS) is a medical device manufactured by KENPAX INTERNATIONAL LIMITED. This product is indexed under FDA Product Code / Category Classification M020199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- OR-1727-WS
- Product Code / EMDN
- M020199
- Device Name
- Operation Room Towel
- Database Sync Date
- 2026-08-09 17:01:42
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 Operation Room Towel?
The registered manufacturer of record for Operation Room Towel is KENPAX INTERNATIONAL LIMITED.
What is the Primary UDI-DI identifier for Operation Room Towel?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 74895237130645.
What classification code is assigned to this device?
This device is registered under product classification code M020199.
Similar Classification Devices (M020199)
Other Devices by KENPAX INTERNATIONAL LIMITED
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