gudid
Primary ID: GL802
V. Mueller (UDI GL802)
Manufactured by STERIS CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for V. Mueller - Primary ID GL802
Device Regulatory Overview
The V. Mueller (Model/Catalog Number: GL802) is a medical device manufactured by STERIS CORPORATION. This product is indexed under FDA Product Code / Category Classification HDE within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- GL802
- Product Code / EMDN
- HDE
- Device Name
- V. Mueller EMMETT TENACULUM HOOK STYLE NO 3 SHARP OVERALL LENGTH 9 inches 22.9CM
- Database Sync Date
- 2026-08-09 10:00:54
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 V. Mueller?
The registered manufacturer of record for V. Mueller is STERIS CORPORATION.
What is the Primary UDI-DI identifier for V. Mueller?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is GL802.
What classification code is assigned to this device?
This device is registered under product classification code HDE.
Similar Classification Devices (HDE)
Other Devices by STERIS CORPORATION
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