GUDIDData
eudamed_udi Primary ID: 04711552925180

STIP (UDI 04711552925180)

Manufactured by Cenefom Corp.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for STIP - Primary ID 04711552925180

Device Regulatory Overview

The STIP (Model/Catalog Number: AS 35129F) is a medical device manufactured by Cenefom Corp.. This product is indexed under FDA Product Code / Category Classification M040799 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
AS 35129F
Product Code / EMDN
M040799
Device Name
ENT Sponge
Database Sync Date
2026-08-09 16:28:46

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 STIP?

The registered manufacturer of record for STIP is Cenefom Corp..

What is the Primary UDI-DI identifier for STIP?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04711552925180.

What classification code is assigned to this device?

This device is registered under product classification code M040799.

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