MIYACATH (UDI 18699415740916)
Manufactured by İstem Medikal Tıbbi Cihaz ve Sanayi Ticaret Anonim Şirketi
Device Regulatory Overview
The MIYACATH (Model/Catalog Number: MYTA-SN 3016) is a medical device manufactured by İstem Medikal Tıbbi Cihaz ve Sanayi Ticaret Anonim Şirketi. This product is indexed under FDA Product Code / Category Classification U01010601 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MYTA-SN 3016
- Product Code / EMDN
- U01010601
- Device Name
- MIYACATH Antibacterial Hydrophilic Urinary Catheter with Water Sachet Tiemann 30 CM 16 CH
- Database Sync Date
- 2026-08-09 16:48:52
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of MIYACATH?
The registered manufacturer of record for MIYACATH is İstem Medikal Tıbbi Cihaz ve Sanayi Ticaret Anonim Şirketi.
What is the Primary UDI-DI identifier for MIYACATH?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 18699415740916.
What classification code is assigned to this device?
This device is registered under product classification code U01010601.
Similar Classification Devices (U01010601)
Other Devices by İstem Medikal Tıbbi Cihaz ve Sanayi Ticaret Anonim Şirketi
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