eudamed_udi Primary ID: 50609244646736

Cutiderm Non-Woven Swabs, Non-Sterile, 10cm x 10cm – 200 Pieces (UDI 50609244646736)

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The Cutiderm Non-Woven Swabs, Non-Sterile, 10cm x 10cm – 200 Pieces (Model/Catalog Number: JF1302) is a medical device manufactured by JFA Medical Ltd.. This product is indexed under FDA Product Code / Category Classification M020299 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: JF1302
Product Code / EMDN: M020299
Device Name: Cutiderm Non-Woven Swabs, Non-Sterile, 10cm x 10cm – 200 Pieces
Database Sync Date: 2026-08-09 16:29:10

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 Cutiderm Non-Woven Swabs, Non-Sterile, 10cm x 10cm – 200 Pieces?

The registered manufacturer of record for Cutiderm Non-Woven Swabs, Non-Sterile, 10cm x 10cm – 200 Pieces is JFA Medical Ltd..

What is the Primary UDI-DI identifier for Cutiderm Non-Woven Swabs, Non-Sterile, 10cm x 10cm – 200 Pieces?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 50609244646736.

What classification code is assigned to this device?

This device is registered under product classification code M020299.

Similar Classification Devices (M020299)

Other Devices by JFA Medical Ltd.

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