Lorski (UDI 315cm)
Manufactured by Shandong Zhushi Pharmaceutical Group Co., Ltd. First Office
Device Regulatory Overview
The Lorski (Model/Catalog Number: 315cm) is a medical device manufactured by Shandong Zhushi Pharmaceutical Group Co., Ltd. First Office. This product is indexed under FDA Product Code / Category Classification MDA within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 315cm
- Product Code / EMDN
- MDA
- Device Name
- lintended Usel:It is used to assist in imnroving skin Pathological scars and assist in preventing the formation of skin pathological scars, not for unhealed wounds.
- Database Sync Date
- 2026-08-09 09:04:48
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 Lorski?
The registered manufacturer of record for Lorski is Shandong Zhushi Pharmaceutical Group Co., Ltd. First Office.
What is the Primary UDI-DI identifier for Lorski?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 315cm.
What classification code is assigned to this device?
This device is registered under product classification code MDA.
Similar Classification Devices (MDA)
Other Devices by Shandong Zhushi Pharmaceutical Group Co., Ltd. First Office
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