Unspecified Brand (UDI 06949517007062)
Manufactured by Shandong Lianfa Medical Plastic Products Co.,Ltd.
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: PA 21G 1.8mm) is a medical device manufactured by Shandong Lianfa Medical Plastic Products 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
- PA 21G 1.8mm
- Product Code / EMDN
- V010401
- Device Name
- safety lancets
- Database Sync Date
- 2026-08-09 16:45:05
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 Shandong Lianfa Medical Plastic Products 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 06949517007062.
What classification code is assigned to this device?
This device is registered under product classification code V010401.
Similar Classification Devices (V010401)
Other Devices by Shandong Lianfa Medical Plastic Products Co.,Ltd.
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