eudamed_udi
Primary ID: 08800076701007
Hemonitor H1 (UDI 08800076701007)
Manufactured by GenBody Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Hemonitor H1 - Primary ID 08800076701007
Device Regulatory Overview
The Hemonitor H1 (Model/Catalog Number: HMGA101) is a medical device manufactured by GenBody Inc.. This product is indexed under FDA Product Code / Category Classification W02029099 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HMGA101
- Product Code / EMDN
- W02029099
- Device Name
- Hemonitor H1
- Database Sync Date
- 2026-08-09 17:16:56
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?
The registered manufacturer of record for Hemonitor H1 is GenBody Inc..
What is the Primary UDI-DI identifier for Hemonitor H1?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08800076701007.
What classification code is assigned to this device?
This device is registered under product classification code W02029099.
Similar Classification Devices (W02029099)
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