gudid
Primary ID: SBPF1713
ParaPost FiberLux (UDI SBPF1713)
Manufactured by COLTENE/WHALEDENT INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ParaPost FiberLux - Primary ID SBPF1713
Device Regulatory Overview
The ParaPost FiberLux (Model/Catalog Number: SBPF1713) is a medical device manufactured by COLTENE/WHALEDENT INC. This product is indexed under FDA Product Code / Category Classification ELR within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SBPF1713
- Product Code / EMDN
- ELR
- Device Name
- STERILE PARAPOST FIBERLUXSIZE 3
- Database Sync Date
- 2026-08-09 09:03:05
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 ParaPost FiberLux?
The registered manufacturer of record for ParaPost FiberLux is COLTENE/WHALEDENT INC.
What is the Primary UDI-DI identifier for ParaPost FiberLux?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SBPF1713.
What classification code is assigned to this device?
This device is registered under product classification code ELR.
Similar Classification Devices (ELR)
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