gudid
Primary ID: 10-91; 10-91K
Nuprep Skin Prep Gel (UDI 10-91; 10-91K)
Manufactured by D. O. WEAVER AND COMPANY
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Nuprep Skin Prep Gel - Primary ID 10-91; 10-91K
Device Regulatory Overview
The Nuprep Skin Prep Gel (Model/Catalog Number: 10-91; 10-91K) is a medical device manufactured by D. O. WEAVER AND COMPANY. This product is indexed under FDA Product Code / Category Classification DRX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 10-91; 10-91K
- Product Code / EMDN
- DRX
- Device Name
- Single-use cup of Nuprep Skin Prep Gel (unit of use)
- Database Sync Date
- 2026-08-09 09:46:58
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 Nuprep Skin Prep Gel?
The registered manufacturer of record for Nuprep Skin Prep Gel is D. O. WEAVER AND COMPANY.
What is the Primary UDI-DI identifier for Nuprep Skin Prep Gel?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10-91; 10-91K.
What classification code is assigned to this device?
This device is registered under product classification code DRX.
Similar Classification Devices (DRX)
Other Devices by D. O. WEAVER AND COMPANY
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