gudid
Primary ID: 982-03976-000
Spectrum, Inc. (UDI 982-03976-000)
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 982-03976-000
Device Regulatory Overview
The Spectrum, Inc. (Model/Catalog Number: 982-03976-000) is a medical device manufactured by SPECTRUM, INC.. This product is indexed under FDA Product Code / Category Classification KKX within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 982-03976-000
- Product Code / EMDN
- KKX
- Device Name
- Sterile Equipment Drape, Robotic Stow Arm, 18"X78"
- Database Sync Date
- 2026-08-09 09:49:39
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 982-03976-000.
What classification code is assigned to this device?
This device is registered under product classification code KKX.
Similar Classification Devices (KKX)
Other Devices by SPECTRUM, INC.
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