HSS 1625, Lifescan Labs USA (UDI 90.2062.057)
Manufactured by Sarstedt Aktiengesellschaft & Co.KG
Device Regulatory Overview
The HSS 1625, Lifescan Labs USA (Model/Catalog Number: 90.2062.057) is a medical device manufactured by Sarstedt Aktiengesellschaft & Co.KG. This product is indexed under FDA Product Code / Category Classification LXG within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 90.2062.057
- Product Code / EMDN
- LXG
- Device Name
- Database Sync Date
- 2026-08-09 09:46:24
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 HSS 1625, Lifescan Labs USA?
The registered manufacturer of record for HSS 1625, Lifescan Labs USA is Sarstedt Aktiengesellschaft & Co.KG.
What is the Primary UDI-DI identifier for HSS 1625, Lifescan Labs USA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 90.2062.057.
What classification code is assigned to this device?
This device is registered under product classification code LXG.
Similar Classification Devices (LXG)
Other Devices by Sarstedt Aktiengesellschaft & Co.KG
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