PROTEXIS (UDI 2D72LS85)
Manufactured by Cardinal Health 200, LLC
Device Regulatory Overview
The PROTEXIS (Model/Catalog Number: 2D72LS85) is a medical device manufactured by Cardinal Health 200, LLC. This product is indexed under FDA Product Code / Category Classification KGO within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- 2D72LS85
- Product Code / EMDN
- KGO
- Device Name
- Sterile Latex Powder Free Surgical Gloves with Hydrogel Coating
- Database Sync Date
- 2026-08-09 09:00:28
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 PROTEXIS?
The registered manufacturer of record for PROTEXIS is Cardinal Health 200, LLC.
What is the Primary UDI-DI identifier for PROTEXIS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 2D72LS85.
What classification code is assigned to this device?
This device is registered under product classification code KGO.
Similar Classification Devices (KGO)
Other Devices by Cardinal Health 200, LLC
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