gudid
Primary ID: 083
DELTA 30 (UDI 083)
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 DELTA 30 - Primary ID 083
Device Regulatory Overview
The DELTA 30 (Model/Catalog Number: 083) 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
- 083
- 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 DELTA 30?
The registered manufacturer of record for DELTA 30 is Heine Optotechnik GmbH & Co. KG.
What is the Primary UDI-DI identifier for DELTA 30?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 083.
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
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