gudid
Primary ID: 3,5 V
K 180 OPHTHALMOSCOPE (UDI 3,5 V)
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 K 180 OPHTHALMOSCOPE - Primary ID 3,5 V
Device Regulatory Overview
The K 180 OPHTHALMOSCOPE (Model/Catalog Number: 3,5 V) 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
- 3,5 V
- 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 K 180 OPHTHALMOSCOPE?
The registered manufacturer of record for K 180 OPHTHALMOSCOPE is Heine Optotechnik GmbH & Co. KG.
What is the Primary UDI-DI identifier for K 180 OPHTHALMOSCOPE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 3,5 V.
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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