gudid
Primary ID: C01251
IOPS Viewpoint (UDI C01251)
Manufactured by Centerline Biomedical, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for IOPS Viewpoint - Primary ID C01251
Device Regulatory Overview
The IOPS Viewpoint (Model/Catalog Number: C01251) is a medical device manufactured by Centerline Biomedical, Inc.. This product is indexed under FDA Product Code / Category Classification DQK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- C01251
- Product Code / EMDN
- DQK
- Device Name
- Simple Curve Catheter, 125 cm
- Database Sync Date
- 2026-08-09 09:13:48
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 IOPS Viewpoint?
The registered manufacturer of record for IOPS Viewpoint is Centerline Biomedical, Inc..
What is the Primary UDI-DI identifier for IOPS Viewpoint?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is C01251.
What classification code is assigned to this device?
This device is registered under product classification code DQK.
Similar Classification Devices (DQK)
Other Devices by Centerline Biomedical, Inc.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint