gudid
Primary ID: Push-Pull
Bioclear Instrument (UDI Push-Pull)
Manufactured by Bioclear Matrix Systems
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Bioclear Instrument - Primary ID Push-Pull
Device Regulatory Overview
The Bioclear Instrument (Model/Catalog Number: Push-Pull) is a medical device manufactured by Bioclear Matrix Systems. This product is indexed under FDA Product Code / Category Classification DZN within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Push-Pull
- Product Code / EMDN
- DZN
- Device Name
- Metal instrument used in dental restorations.
- Database Sync Date
- 2026-08-09 09:01:11
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 Bioclear Instrument?
The registered manufacturer of record for Bioclear Instrument is Bioclear Matrix Systems.
What is the Primary UDI-DI identifier for Bioclear Instrument?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is Push-Pull.
What classification code is assigned to this device?
This device is registered under product classification code DZN.
Similar Classification Devices (DZN)
Other Devices by Bioclear Matrix Systems
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint