gudid
Primary ID: 985-03502-000
Spectrum, Inc. (UDI 985-03502-000)
Manufactured by SPECTRUM, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Spectrum, Inc. - Primary ID 985-03502-000
Device Regulatory Overview
The Spectrum, Inc. (Model/Catalog Number: 985-03502-000) is a medical device manufactured by SPECTRUM, INC.. This product is indexed under FDA Product Code / Category Classification FQL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 985-03502-000
- Product Code / EMDN
- FQL
- Device Name
- Stockinette- 50/50% - Bias, 4" X 3 Yards - Sterile
- Database Sync Date
- 2026-08-09 09:49:29
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 Spectrum, Inc.?
The registered manufacturer of record for Spectrum, Inc. is SPECTRUM, INC..
What is the Primary UDI-DI identifier for Spectrum, Inc.?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 985-03502-000.
What classification code is assigned to this device?
This device is registered under product classification code FQL.
Similar Classification Devices (FQL)
Other Devices by SPECTRUM, INC.
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