eudamed_udi
Primary ID: 08809964140218
Oxygen Therapy Chamber Lower Extremity Boot (UDI 08809964140218)
Manufactured by GHC Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Oxygen Therapy Chamber Lower Extremity Boot - Primary ID 08809964140218
Device Regulatory Overview
The Oxygen Therapy Chamber Lower Extremity Boot (Model/Catalog Number: O2TEC1) is a medical device manufactured by GHC Co., Ltd.. This product is indexed under FDA Product Code / Category Classification R03010207 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- O2TEC1
- Product Code / EMDN
- R03010207
- Device Name
- Oxygen Therapy Chamber Lower Extremity Boot
- Database Sync Date
- 2026-08-09 16:50:51
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 Oxygen Therapy Chamber Lower Extremity Boot?
The registered manufacturer of record for Oxygen Therapy Chamber Lower Extremity Boot is GHC Co., Ltd..
What is the Primary UDI-DI identifier for Oxygen Therapy Chamber Lower Extremity Boot?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08809964140218.
What classification code is assigned to this device?
This device is registered under product classification code R03010207.
Similar Classification Devices (R03010207)
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