gudid
Primary ID: 166
HEINE K180 Diagnostic Set (UDI 166)
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 HEINE K180 Diagnostic Set - Primary ID 166
Device Regulatory Overview
The HEINE K180 Diagnostic Set (Model/Catalog Number: 166) is a medical device manufactured by Heine Optotechnik GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification HLJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 166
- Product Code / EMDN
- HLJ
- 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 HEINE K180 Diagnostic Set?
The registered manufacturer of record for HEINE K180 Diagnostic Set is Heine Optotechnik GmbH & Co. KG.
What is the Primary UDI-DI identifier for HEINE K180 Diagnostic Set?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 166.
What classification code is assigned to this device?
This device is registered under product classification code HLJ.
Similar Classification Devices (HLJ)
Other Devices by Heine Optotechnik GmbH & Co. KG
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