gudid
Primary ID: PROSNCG-L
PROTECT 800 (UDI PROSNCG-L)
Manufactured by McGowan Enterprises, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PROTECT 800 - Primary ID PROSNCG-L
Device Regulatory Overview
The PROTECT 800 (Model/Catalog Number: PROSNCG-L) is a medical device manufactured by McGowan Enterprises, Inc.. This product is indexed under FDA Product Code / Category Classification OPJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PROSNCG-L
- Product Code / EMDN
- OPJ
- Device Name
- SURGICAL GLOVE, STERILE, NITRILE, 12" LENGTH, CHEMO TESTED, POWDER FREE, WHITE, LARGE
- Database Sync Date
- 2026-08-09 09:08:46
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 PROTECT 800?
The registered manufacturer of record for PROTECT 800 is McGowan Enterprises, Inc..
What is the Primary UDI-DI identifier for PROTECT 800?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PROSNCG-L.
What classification code is assigned to this device?
This device is registered under product classification code OPJ.
Similar Classification Devices (OPJ)
Other Devices by McGowan Enterprises, Inc.
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