gudid
Primary ID: 987-03604.000
Spectrum, Inc. (UDI 987-03604.000)
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 987-03604.000
Device Regulatory Overview
The Spectrum, Inc. (Model/Catalog Number: 987-03604.000) is a medical device manufactured by SPECTRUM, INC.. This product is indexed under FDA Product Code / Category Classification FQM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 987-03604.000
- Product Code / EMDN
- FQM
- Device Name
- Non-Sterile Pressure Bandage, Esmarch, 6" x 12'
- Database Sync Date
- 2026-08-09 09:49:39
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
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 987-03604.000.
What classification code is assigned to this device?
This device is registered under product classification code FQM.
Similar Classification Devices (FQM)
Other Devices by SPECTRUM, INC.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint