gudid
Primary ID: BPSYRNDL2
BioPure (UDI BPSYRNDL2)
Manufactured by TULSA DENTAL PRODUCTS LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for BioPure - Primary ID BPSYRNDL2
Device Regulatory Overview
The BioPure (Model/Catalog Number: BPSYRNDL2) is a medical device manufactured by TULSA DENTAL PRODUCTS LLC. This product is indexed under FDA Product Code / Category Classification KJJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BPSYRNDL2
- Product Code / EMDN
- KJJ
- Device Name
- BioPure MTAD Endo Starter System L
- Database Sync Date
- 2026-08-09 09:15:06
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 BioPure?
The registered manufacturer of record for BioPure is TULSA DENTAL PRODUCTS LLC.
What is the Primary UDI-DI identifier for BioPure?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is BPSYRNDL2.
What classification code is assigned to this device?
This device is registered under product classification code KJJ.
Similar Classification Devices (KJJ)
Other Devices by TULSA DENTAL PRODUCTS LLC
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