gudid
Primary ID: C701
HiVac 7 (UDI C701)
Manufactured by SUMMIT MEDICAL LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HiVac 7 - Primary ID C701
Device Regulatory Overview
The HiVac 7 (Model/Catalog Number: C701) is a medical device manufactured by SUMMIT MEDICAL LIMITED. This product is indexed under FDA Product Code / Category Classification KIH within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- C701
- Product Code / EMDN
- KIH
- Device Name
- Mixing and Delivery System
- Database Sync Date
- 2026-08-09 09:22:51
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 HiVac 7?
The registered manufacturer of record for HiVac 7 is SUMMIT MEDICAL LIMITED.
What is the Primary UDI-DI identifier for HiVac 7?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is C701.
What classification code is assigned to this device?
This device is registered under product classification code KIH.
Similar Classification Devices (KIH)
Other Devices by SUMMIT MEDICAL LIMITED
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint