gudid
Primary ID: CSFE
CULLUM SINUS FLOOR ELEV KIT (UDI CSFE)
Manufactured by W.H. Holden, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CULLUM SINUS FLOOR ELEV KIT - Primary ID CSFE
Device Regulatory Overview
The CULLUM SINUS FLOOR ELEV KIT (Model/Catalog Number: CSFE) is a medical device manufactured by W.H. Holden, Inc.. This product is indexed under FDA Product Code / Category Classification GFI within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CSFE
- Product Code / EMDN
- GFI
- Device Name
- Database Sync Date
- 2026-08-09 09:01:13
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 CULLUM SINUS FLOOR ELEV KIT?
The registered manufacturer of record for CULLUM SINUS FLOOR ELEV KIT is W.H. Holden, Inc..
What is the Primary UDI-DI identifier for CULLUM SINUS FLOOR ELEV KIT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is CSFE.
What classification code is assigned to this device?
This device is registered under product classification code GFI.
Similar Classification Devices (GFI)
Other Devices by W.H. Holden, Inc.
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