gudid
Primary ID: 90652
B1 REGEN Flowable Composite 4pk of Syringes (UDI 90652)
Manufactured by Vista Dental
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for B1 REGEN Flowable Composite 4pk of Syringes - Primary ID 90652
Device Regulatory Overview
The B1 REGEN Flowable Composite 4pk of Syringes (Model/Catalog Number: 90652) is a medical device manufactured by Vista Dental. This product is indexed under FDA Product Code / Category Classification EBF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 90652
- Product Code / EMDN
- EBF
- Device Name
- Database Sync Date
- 2026-08-09 09:32:54
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 B1 REGEN Flowable Composite 4pk of Syringes?
The registered manufacturer of record for B1 REGEN Flowable Composite 4pk of Syringes is Vista Dental.
What is the Primary UDI-DI identifier for B1 REGEN Flowable Composite 4pk of Syringes?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 90652.
What classification code is assigned to this device?
This device is registered under product classification code EBF.
Similar Classification Devices (EBF)
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