eudamed_udi
Primary ID: 08720299490611
Greenhabit (UDI 08720299490611)
Manufactured by greenhabit BV
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Greenhabit - Primary ID 08720299490611
Device Regulatory Overview
The Greenhabit (Model/Catalog Number: Greenhabit version 1.5) is a medical device manufactured by greenhabit BV. This product is indexed under FDA Product Code / Category Classification V92 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- Greenhabit version 1.5
- Product Code / EMDN
- V92
- Device Name
- Greenhabit
- Database Sync Date
- 2026-08-09 16:28:47
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 Greenhabit?
The registered manufacturer of record for Greenhabit is greenhabit BV.
What is the Primary UDI-DI identifier for Greenhabit?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08720299490611.
What classification code is assigned to this device?
This device is registered under product classification code V92.
Similar Classification Devices (V92)
Other Devices by greenhabit BV
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