eudamed_udi
Primary ID: 06945975822339
LT (UDI 06945975822339)
Manufactured by Shanghai Litu Medical Appliances Co.,Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LT - Primary ID 06945975822339
Device Regulatory Overview
The LT (Model/Catalog Number: PF-3-M) is a medical device manufactured by Shanghai Litu Medical Appliances Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification K02010201 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- PF-3-M
- Product Code / EMDN
- K02010201
- Device Name
- Disposable Neutral Electrode
- Database Sync Date
- 2026-08-09 16:51:53
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 LT?
The registered manufacturer of record for LT is Shanghai Litu Medical Appliances Co.,Ltd..
What is the Primary UDI-DI identifier for LT?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06945975822339.
What classification code is assigned to this device?
This device is registered under product classification code K02010201.
Similar Classification Devices (K02010201)
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