gudid
Primary ID: H01035
IOPS (UDI H01035)
Manufactured by Centerline Biomedical, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for IOPS - Primary ID H01035
Device Regulatory Overview
The IOPS (Model/Catalog Number: H01035) 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
- H01035
- Product Code / EMDN
- DQK
- Device Name
- Guidewire Handle
- 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?
The registered manufacturer of record for IOPS is Centerline Biomedical, Inc..
What is the Primary UDI-DI identifier for IOPS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is H01035.
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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