Lensmeter (UDI SK-1000A)
Manufactured by CHONGQING SUNKINGDOM MEDICAL INSTRUMENT CO.,LTD
Device Regulatory Overview
The Lensmeter (Model/Catalog Number: SK-1000A) is a medical device manufactured by CHONGQING SUNKINGDOM MEDICAL INSTRUMENT CO.,LTD. This product is indexed under FDA Product Code / Category Classification HLM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SK-1000A
- Product Code / EMDN
- HLM
- Device Name
- It is mainly used to measure the vertex power and prism power of various spectacle lenses, determine the position and direction of the column lens axis, print marks on the unprocessed lens, and check whether the lens are correctly installed in the frame
- Database Sync Date
- 2026-08-09 09:06:39
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 Lensmeter?
The registered manufacturer of record for Lensmeter is CHONGQING SUNKINGDOM MEDICAL INSTRUMENT CO.,LTD.
What is the Primary UDI-DI identifier for Lensmeter?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is SK-1000A.
What classification code is assigned to this device?
This device is registered under product classification code HLM.
Similar Classification Devices (HLM)
Other Devices by CHONGQING SUNKINGDOM MEDICAL INSTRUMENT CO.,LTD
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