GUDIDData
eudamed_udi Primary ID: 06958627542707

Vaginal Speculum (UDI 06958627542707)

Manufactured by Ningbo Greetmed Medical Instruments Co.,Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Vaginal Speculum - Primary ID 06958627542707

Device Regulatory Overview

The Vaginal Speculum (Model/Catalog Number: XS) is a medical device manufactured by Ningbo Greetmed Medical Instruments Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification U089006 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
XS
Product Code / EMDN
U089006
Device Name
Vaginal Speculum
Database Sync Date
2026-08-09 17:07:52

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 Vaginal Speculum?

The registered manufacturer of record for Vaginal Speculum is Ningbo Greetmed Medical Instruments Co.,Ltd..

What is the Primary UDI-DI identifier for Vaginal Speculum?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06958627542707.

What classification code is assigned to this device?

This device is registered under product classification code U089006.

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