GUDIDData
eudamed_udi Primary ID: 08698573035981

PLASTI-MED (UDI 08698573035981)

Manufactured by Plasti-med Plastik Medikal Ürünler San. ve Tic. Ltd. Şti.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for PLASTI-MED - Primary ID 08698573035981

Device Regulatory Overview

The PLASTI-MED (Model/Catalog Number: 489 275) is a medical device manufactured by Plasti-med Plastik Medikal Ürünler San. ve Tic. Ltd. Şti.. This product is indexed under FDA Product Code / Category Classification R020106 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
489 275
Product Code / EMDN
R020106
Device Name
BREATHING CIRCUIT EXTENDED IPPB PEDIATRIC SEMI CLOSED SYSTEM
Database Sync Date
2026-08-09 17:06:01

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 PLASTI-MED?

The registered manufacturer of record for PLASTI-MED is Plasti-med Plastik Medikal Ürünler San. ve Tic. Ltd. Şti..

What is the Primary UDI-DI identifier for PLASTI-MED?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08698573035981.

What classification code is assigned to this device?

This device is registered under product classification code R020106.

Similar Classification Devices (R020106)

Other Devices by Plasti-med Plastik Medikal Ürünler San. ve Tic. Ltd. Şti.

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