gudid
Primary ID: PF1715C
ParaPost (UDI PF1715C)
Manufactured by COLTENE/WHALEDENT INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ParaPost - Primary ID PF1715C
Device Regulatory Overview
The ParaPost (Model/Catalog Number: PF1715C) 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
- PF1715C
- Product Code / EMDN
- ELR
- Device Name
- PARAPOST FIBERLUX POSTS SIZE 5
- 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?
The registered manufacturer of record for ParaPost is COLTENE/WHALEDENT INC.
What is the Primary UDI-DI identifier for ParaPost?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is PF1715C.
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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