gudid
Primary ID: C00752
IOPS Viewpoint (UDI C00752)
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 C00752
Device Regulatory Overview
The IOPS Viewpoint (Model/Catalog Number: C00752) 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
- C00752
- Product Code / EMDN
- DQK
- Device Name
- Double Curve Catheter, 75 cm
- Database Sync Date
- 2026-08-09 09:13:48
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 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 C00752.
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.
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