PRIMEDGE (UDI 06951933801346)
Manufactured by Huaian Tianda Medical Instruments Co., Ltd.
Device Regulatory Overview
The PRIMEDGE (Model/Catalog Number: 0403) is a medical device manufactured by Huaian Tianda Medical Instruments Co., Ltd.. This product is indexed under FDA Product Code / Category Classification V010401 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0403
- Product Code / EMDN
- V010401
- Device Name
- Sterile Blood Lancets
- Database Sync Date
- 2026-08-09 17:15:37
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 PRIMEDGE?
The registered manufacturer of record for PRIMEDGE is Huaian Tianda Medical Instruments Co., Ltd..
What is the Primary UDI-DI identifier for PRIMEDGE?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06951933801346.
What classification code is assigned to this device?
This device is registered under product classification code V010401.
Similar Classification Devices (V010401)
Other Devices by Huaian Tianda Medical Instruments Co., Ltd.
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