gudid
Primary ID: SBP6845
ParaPost XT (UDI SBP6845)
Manufactured by COLTENE/WHALEDENT INC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ParaPost XT - Primary ID SBP6845
Device Regulatory Overview
The ParaPost XT (Model/Catalog Number: SBP6845) 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
- SBP6845
- Product Code / EMDN
- ELR
- Device Name
- STERILE PARAPOST XT SIZE 4.5
- 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 XT?
The registered manufacturer of record for ParaPost XT is COLTENE/WHALEDENT INC.
What is the Primary UDI-DI identifier for ParaPost XT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SBP6845.
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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