GUDIDData
gudid Primary ID: 32310007

SYMBIOS (UDI 32310007)

Manufactured by COLLAGEN MATRIX, INC.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SYMBIOS - Primary ID 32310007

Device Regulatory Overview

The SYMBIOS (Model/Catalog Number: 32310007) is a medical device manufactured by COLLAGEN MATRIX, INC.. This product is indexed under FDA Product Code / Category Classification NPM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
32310007
Product Code / EMDN
NPM
Device Name
Xenograft Granules Syringe 0.5cc, Particle Size 0.25 - 1.0mm
Database Sync Date
2026-08-09 09:14:39

Full Regulatory Attributes

🔒 Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of SYMBIOS?

The registered manufacturer of record for SYMBIOS is COLLAGEN MATRIX, INC..

What is the Primary UDI-DI identifier for SYMBIOS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 32310007.

What classification code is assigned to this device?

This device is registered under product classification code NPM.

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