gudid
Primary ID: SBP6855
ParaPost XT (UDI SBP6855)
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 SBP6855
Device Regulatory Overview
The ParaPost XT (Model/Catalog Number: SBP6855) 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
- SBP6855
- Product Code / EMDN
- ELR
- Device Name
- STERILE PARAPOST XT SIZE 5.5
- Database Sync Date
- 2026-08-09 09:03:05
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
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 SBP6855.
What classification code is assigned to this device?
This device is registered under product classification code ELR.
Similar Classification Devices (ELR)
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint