gudid
Primary ID: HC702-180
Pointe Scientific, Inc. (UDI HC702-180)
Manufactured by HORIBA INSTRUMENTS INCORPORATED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Pointe Scientific, Inc. - Primary ID HC702-180
Device Regulatory Overview
The Pointe Scientific, Inc. (Model/Catalog Number: HC702-180) is a medical device manufactured by HORIBA INSTRUMENTS INCORPORATED. This product is indexed under FDA Product Code / Category Classification KHS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HC702-180
- Product Code / EMDN
- KHS
- Device Name
- Carbon Dioxide Liquid Reagent, for the quantitative determination of Carbon Dioxide in serum. For in vitro diagnostic use. 4 x 45mL
- Database Sync Date
- 2026-08-09 09:22:13
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 Pointe Scientific, Inc.?
The registered manufacturer of record for Pointe Scientific, Inc. is HORIBA INSTRUMENTS INCORPORATED.
What is the Primary UDI-DI identifier for Pointe Scientific, Inc.?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is HC702-180.
What classification code is assigned to this device?
This device is registered under product classification code KHS.
Similar Classification Devices (KHS)
Other Devices by HORIBA INSTRUMENTS INCORPORATED
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint