GUDIDData
eudamed_udi Primary ID: 06923310905480

Insufflation Tube (UDI 06923310905480)

Manufactured by Hangzhou Formed Medical Devices Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Insufflation Tube - Primary ID 06923310905480

Device Regulatory Overview

The Insufflation Tube (Model/Catalog Number: PS010101) is a medical device manufactured by Hangzhou Formed Medical Devices Co., Ltd.. This product is indexed under FDA Product Code / Category Classification K01020120 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
PS010101
Product Code / EMDN
K01020120
Device Name
Insufflation Tube
Database Sync Date
2026-08-09 17:31:46

Full Regulatory Attributes

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{
    "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 Insufflation Tube?

The registered manufacturer of record for Insufflation Tube is Hangzhou Formed Medical Devices Co., Ltd..

What is the Primary UDI-DI identifier for Insufflation Tube?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06923310905480.

What classification code is assigned to this device?

This device is registered under product classification code K01020120.

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