eudamed_udi
Primary ID: 05420040819892
SAFETOUCH DIALYSIS CATH PLUS (UDI 05420040819892)
Manufactured by NIPRO CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for SAFETOUCH DIALYSIS CATH PLUS - Primary ID 05420040819892
Device Regulatory Overview
The SAFETOUCH DIALYSIS CATH PLUS (Model/Catalog Number: AVSF-CATHP-1638-GJ) is a medical device manufactured by NIPRO CORPORATION. This product is indexed under FDA Product Code / Category Classification F900201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- AVSF-CATHP-1638-GJ
- Product Code / EMDN
- F900201
- Device Name
- SAFETY HEMODIALYSIS NEEDLE
- Database Sync Date
- 2026-08-09 17:17:37
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 SAFETOUCH DIALYSIS CATH PLUS?
The registered manufacturer of record for SAFETOUCH DIALYSIS CATH PLUS is NIPRO CORPORATION.
What is the Primary UDI-DI identifier for SAFETOUCH DIALYSIS CATH PLUS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05420040819892.
What classification code is assigned to this device?
This device is registered under product classification code F900201.
Similar Classification Devices (F900201)
Other Devices by NIPRO CORPORATION
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