eudamed_udi
Primary ID: 06975871860494
Unspecified Brand (UDI 06975871860494)
Manufactured by Ningbo KK-Bioscience Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Unspecified Brand - Primary ID 06975871860494
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: H3) is a medical device manufactured by Ningbo KK-Bioscience Co., Ltd.. This product is indexed under FDA Product Code / Category Classification B0499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- H3
- Product Code / EMDN
- B0499
- Device Name
- Reusable pressure infusor
- Database Sync Date
- 2026-08-09 17:33:24
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Ningbo KK-Bioscience Co., Ltd..
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975871860494.
What classification code is assigned to this device?
This device is registered under product classification code B0499.
Similar Classification Devices (B0499)
Other Devices by Ningbo KK-Bioscience Co., Ltd.
Programmatic Export
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