eudamed_udi
Primary ID: 04250326800457
Unspecified Brand (UDI 04250326800457)
Manufactured by Albert Heiss GmbH & Co. KG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 04250326800457
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: H-1071) is a medical device manufactured by Albert Heiss GmbH & Co. KG. This product is indexed under FDA Product Code / Category Classification L170102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- H-1071
- Product Code / EMDN
- L170102
- Device Name
- Eye Speculum
- Database Sync Date
- 2026-08-09 16:29:11
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Albert Heiss GmbH & Co. KG.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250326800457.
What classification code is assigned to this device?
This device is registered under product classification code L170102.
Similar Classification Devices (L170102)
Other Devices by Albert Heiss GmbH & Co. KG
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