GUDIDData
gudid Primary ID: WALDMANN EPISIOTOMY SCISSORS

SCISSORS (UDI WALDMANN EPISIOTOMY SCISSORS)

Manufactured by DR.FRIGZ INTERNATIONAL(PVT)LTD,

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

Device Regulatory Overview

The SCISSORS (Model/Catalog Number: WALDMANN EPISIOTOMY SCISSORS) is a medical device manufactured by DR.FRIGZ INTERNATIONAL(PVT)LTD,. This product is indexed under FDA Product Code / Category Classification KOH within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
WALDMANN EPISIOTOMY SCISSORS
Product Code / EMDN
KOH
Device Name
WALDMANN EPISIOTOMY SCISSORS, 7-1/4"
Database Sync Date
2026-08-09 09:06:20

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 SCISSORS?

The registered manufacturer of record for SCISSORS is DR.FRIGZ INTERNATIONAL(PVT)LTD,.

What is the Primary UDI-DI identifier for SCISSORS?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is WALDMANN EPISIOTOMY SCISSORS.

What classification code is assigned to this device?

This device is registered under product classification code KOH.

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