GUDIDData
gudid Primary ID: 453A

VISORB (UDI 453A)

Manufactured by C.P. MEDICAL CORPORATION

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VISORB - Primary ID 453A

Device Regulatory Overview

The VISORB (Model/Catalog Number: 453A) is a medical device manufactured by C.P. MEDICAL CORPORATION. This product is indexed under FDA Product Code / Category Classification GAM within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
453A
Product Code / EMDN
GAM
Device Name
Suture
Database Sync Date
2026-08-09 09:12:05

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 VISORB?

The registered manufacturer of record for VISORB is C.P. MEDICAL CORPORATION.

What is the Primary UDI-DI identifier for VISORB?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 453A.

What classification code is assigned to this device?

This device is registered under product classification code GAM.

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