eudamed_udi
Primary ID: 08800076700451
HelicoSign Dry (UDI 08800076700451)
Manufactured by GenBody Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for HelicoSign Dry - Primary ID 08800076700451
Device Regulatory Overview
The HelicoSign Dry (Model/Catalog Number: HPYD050) is a medical device manufactured by GenBody Inc.. This product is indexed under FDA Product Code / Category Classification W0105010499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- HPYD050
- Product Code / EMDN
- W0105010499
- Device Name
- Helicosign Dry
- Database Sync Date
- 2026-08-09 19:06:33
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 HelicoSign Dry?
The registered manufacturer of record for HelicoSign Dry is GenBody Inc..
What is the Primary UDI-DI identifier for HelicoSign Dry?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08800076700451.
What classification code is assigned to this device?
This device is registered under product classification code W0105010499.
Similar Classification Devices (W0105010499)
Other Devices by GenBody Inc.
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