HOMECATH (UDI 18699415739897)
Manufactured by İstem Medikal Tıbbi Cihaz ve Sanayi Ticaret Anonim Şirketi
Device Regulatory Overview
The HOMECATH (Model/Catalog Number: HCT-RU 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
- HCT-RU 3016
- Product Code / EMDN
- U01010601
- Device Name
- HOMECATH Hydrophilic Urinary Catheter -Ready To Use Tiemann 30 CM 16 CH Aluminum Package
- Database Sync Date
- 2026-08-09 16:46:38
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 HOMECATH?
The registered manufacturer of record for HOMECATH is İstem Medikal Tıbbi Cihaz ve Sanayi Ticaret Anonim Şirketi.
What is the Primary UDI-DI identifier for HOMECATH?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 18699415739897.
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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