eudamed_udi
Primary ID: D-8698940540919JK
MORTON MEDICAL (UDI D-8698940540919JK)
Manufactured by Morton Medikal San ve Tic A.Ş.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MORTON MEDICAL - Primary ID D-8698940540919JK
Device Regulatory Overview
The MORTON MEDICAL (Model/Catalog Number: MN 103-09) is a medical device manufactured by Morton Medikal San ve Tic A.Ş.. This product is indexed under FDA Product Code / Category Classification R02010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MN 103-09
- Product Code / EMDN
- R02010102
- Device Name
- ANESTHESIA CIRCUIT WITH ONE WATER TRAP AND 100CM. EXRTA LIMB, PEDIATRIC
- Database Sync Date
- 2026-08-09 16:46:12
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of MORTON MEDICAL?
The registered manufacturer of record for MORTON MEDICAL is Morton Medikal San ve Tic A.Ş..
What is the Primary UDI-DI identifier for MORTON MEDICAL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-8698940540919JK.
What classification code is assigned to this device?
This device is registered under product classification code R02010102.
Similar Classification Devices (R02010102)
Other Devices by Morton Medikal San ve Tic A.Ş.
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