GUDIDData
eudamed_udi Primary ID: 06438129352122

SELEFA®Surgical tape PE-film, transparent, 2,5 cm x 9,1 m (UDI 06438129352122)

Manufactured by OneMed Group Oy

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SELEFA®Surgical tape PE-film, transparent, 2,5 cm x 9,1 m - Primary ID 06438129352122

Device Regulatory Overview

The SELEFA®Surgical tape PE-film, transparent, 2,5 cm x 9,1 m (Model/Catalog Number: 2402032) is a medical device manufactured by OneMed Group Oy. This product is indexed under FDA Product Code / Category Classification M050101 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
2402032
Product Code / EMDN
M050101
Device Name
Self-adhesive Dressings, non-sterile
Database Sync Date
2026-08-09 16:30:19

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 SELEFA®Surgical tape PE-film, transparent, 2,5 cm x 9,1 m?

The registered manufacturer of record for SELEFA®Surgical tape PE-film, transparent, 2,5 cm x 9,1 m is OneMed Group Oy.

What is the Primary UDI-DI identifier for SELEFA®Surgical tape PE-film, transparent, 2,5 cm x 9,1 m?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06438129352122.

What classification code is assigned to this device?

This device is registered under product classification code M050101.

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