GUDIDData
eudamed_udi Primary ID: 06134473000053

STERIPAD (UDI 06134473000053)

Manufactured by SARL CICRETES

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for STERIPAD - Primary ID 06134473000053

Device Regulatory Overview

The STERIPAD (Model/Catalog Number: 03010) is a medical device manufactured by SARL CICRETES. This product is indexed under FDA Product Code / Category Classification M0299 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
03010
Product Code / EMDN
M0299
Device Name
sterile gauze
Database Sync Date
2026-08-09 16:29:44

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 STERIPAD?

The registered manufacturer of record for STERIPAD is SARL CICRETES.

What is the Primary UDI-DI identifier for STERIPAD?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06134473000053.

What classification code is assigned to this device?

This device is registered under product classification code M0299.

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