Unspecified Brand (UDI 36979956139384)
Manufactured by Jiangsu Greatwall Medical Devices Co., Ltd.
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: CARTON SUKKI 30G8) is a medical device manufactured by Jiangsu Greatwall Medical Devices Co., Ltd.. This product is indexed under FDA Product Code / Category Classification A0101010102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CARTON SUKKI 30G8
- Product Code / EMDN
- A0101010102
- Device Name
- HYPODERMIC NEEDLES FOR SINGLE USE
- Database Sync Date
- 2026-08-09 16:29:00
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 Jiangsu Greatwall Medical Devices 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 36979956139384.
What classification code is assigned to this device?
This device is registered under product classification code A0101010102.
Similar Classification Devices (A0101010102)
Other Devices by Jiangsu Greatwall Medical Devices Co., Ltd.
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