eudamed_udi
Primary ID: 08800076701199
Hemonitor H1 microcuvette (UDI 08800076701199)
Manufactured by GenBody Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Hemonitor H1 microcuvette - Primary ID 08800076701199
Device Regulatory Overview
The Hemonitor H1 microcuvette (Model/Catalog Number: HMAC050) is a medical device manufactured by GenBody Inc.. This product is indexed under FDA Product Code / Category Classification W0503010203 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HMAC050
- Product Code / EMDN
- W0503010203
- Device Name
- Hemonitor H1 microcuvette
- Database Sync Date
- 2026-08-09 16:46:36
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 Hemonitor H1 microcuvette?
The registered manufacturer of record for Hemonitor H1 microcuvette is GenBody Inc..
What is the Primary UDI-DI identifier for Hemonitor H1 microcuvette?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08800076701199.
What classification code is assigned to this device?
This device is registered under product classification code W0503010203.
Similar Classification Devices (W0503010203)
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