eudamed_udi
Primary ID: 05420040819175
CURACASE (UDI 05420040819175)
Manufactured by NIPRO CORPORATION
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for CURACASE - Primary ID 05420040819175
Device Regulatory Overview
The CURACASE (Model/Catalog Number: ZT002-009-0001-015) is a medical device manufactured by NIPRO CORPORATION. This product is indexed under FDA Product Code / Category Classification A0101010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ZT002-009-0001-015
- Product Code / EMDN
- A0101010102
- Device Name
- NEEDLE
- Database Sync Date
- 2026-08-09 16:29:04
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 CURACASE?
The registered manufacturer of record for CURACASE is NIPRO CORPORATION.
What is the Primary UDI-DI identifier for CURACASE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05420040819175.
What classification code is assigned to this device?
This device is registered under product classification code A0101010102.
Similar Classification Devices (A0101010102)
Other Devices by NIPRO CORPORATION
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