eudamed_udi
Primary ID: 74895237108736
Scrub Suit (UDI 74895237108736)
Manufactured by KENPAX INTERNATIONAL LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Scrub Suit - Primary ID 74895237108736
Device Regulatory Overview
The Scrub Suit (Model/Catalog Number: 68-7175-B) is a medical device manufactured by KENPAX INTERNATIONAL LIMITED. This product is indexed under FDA Product Code / Category Classification T0205 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 68-7175-B
- Product Code / EMDN
- T0205
- Device Name
- Scrub Suit
- Database Sync Date
- 2026-08-09 16:47:29
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 Scrub Suit?
The registered manufacturer of record for Scrub Suit is KENPAX INTERNATIONAL LIMITED.
What is the Primary UDI-DI identifier for Scrub Suit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 74895237108736.
What classification code is assigned to this device?
This device is registered under product classification code T0205.
Similar Classification Devices (T0205)
Other Devices by KENPAX INTERNATIONAL LIMITED
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