ORYA (UDI 06958888002101)
Manufactured by Nantong City YOJO Medical Products Co., Ltd.
Device Regulatory Overview
The ORYA (Model/Catalog Number: 55x17mm（pink）) is a medical device manufactured by Nantong City YOJO Medical Products Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Q030199 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 55x17mm（pink）
- Product Code / EMDN
- Q030199
- Device Name
- Nasal strips
- Database Sync Date
- 2026-08-09 16:45:49
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 ORYA?
The registered manufacturer of record for ORYA is Nantong City YOJO Medical Products Co., Ltd..
What is the Primary UDI-DI identifier for ORYA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06958888002101.
What classification code is assigned to this device?
This device is registered under product classification code Q030199.
Similar Classification Devices (Q030199)
Other Devices by Nantong City YOJO Medical Products Co., Ltd.
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