gudid
Primary ID: DG2M-330
Spectrum, Inc. (UDI DG2M-330)
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 DG2M-330
Device Regulatory Overview
The Spectrum, Inc. (Model/Catalog Number: DG2M-330) is a medical device manufactured by SPECTRUM, INC.. This product is indexed under FDA Product Code / Category Classification FPB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- DG2M-330
- Product Code / EMDN
- FPB
- Device Name
- Hydrophilic Syringe Tip Filter - DG2M-330-100, Non- Sterile
- 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 DG2M-330.
What classification code is assigned to this device?
This device is registered under product classification code FPB.
Similar Classification Devices (FPB)
Other Devices by SPECTRUM, INC.
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