gudid
Primary ID: 000
iC1 (UDI 000)
Manufactured by Heine Optotechnik GmbH & Co. KG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for iC1 - Primary ID 000
Device Regulatory Overview
The iC1 (Model/Catalog Number: 000) is a medical device manufactured by Heine Optotechnik GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification KYT within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 000
- Product Code / EMDN
- KYT
- Device Name
- Database Sync Date
- 2026-08-09 09:26:12
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 iC1?
The registered manufacturer of record for iC1 is Heine Optotechnik GmbH & Co. KG.
What is the Primary UDI-DI identifier for iC1?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 000.
What classification code is assigned to this device?
This device is registered under product classification code KYT.
Similar Classification Devices (KYT)
Other Devices by Heine Optotechnik GmbH & Co. KG
Programmatic Export
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