PURIFIER H 200 Synthetic High Flux Dialyser (UDI 08697658015733)
Manufactured by FARMASOL TIBBİ ÜRÜNLER SAN. VE TİC. A.Ş.
Device Regulatory Overview
The PURIFIER H 200 Synthetic High Flux Dialyser (Model/Catalog Number: PURIFIER HIGH FLUX H 200 DIALYSER) is a medical device manufactured by FARMASOL TIBBİ ÜRÜNLER SAN. VE TİC. A.Ş.. This product is indexed under FDA Product Code / Category Classification F01060303 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PURIFIER HIGH FLUX H 200 DIALYSER
- Product Code / EMDN
- F01060303
- Device Name
- PURIFIER H 200 Synthetic High Flux Dialyser
- Database Sync Date
- 2026-08-09 16:30:10
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of PURIFIER H 200 Synthetic High Flux Dialyser?
The registered manufacturer of record for PURIFIER H 200 Synthetic High Flux Dialyser is FARMASOL TIBBİ ÜRÜNLER SAN. VE TİC. A.Ş..
What is the Primary UDI-DI identifier for PURIFIER H 200 Synthetic High Flux Dialyser?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08697658015733.
What classification code is assigned to this device?
This device is registered under product classification code F01060303.
Similar Classification Devices (F01060303)
Other Devices by FARMASOL TIBBİ ÜRÜNLER SAN. VE TİC. A.Ş.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint