Canister (UDI 06975984060781)
Manufactured by Shenzhen Lifotronic Technology Co., Ltd.
Device Regulatory Overview
The Canister (Model/Catalog Number: CL1000) is a medical device manufactured by Shenzhen Lifotronic Technology Co., Ltd.. This product is indexed under FDA Product Code / Category Classification Z12019085 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- CL1000
- Product Code / EMDN
- Z12019085
- Device Name
- Canister
- Database Sync Date
- 2026-08-09 18:09:53
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 Canister?
The registered manufacturer of record for Canister is Shenzhen Lifotronic Technology Co., Ltd..
What is the Primary UDI-DI identifier for Canister?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06975984060781.
What classification code is assigned to this device?
This device is registered under product classification code Z12019085.
Similar Classification Devices (Z12019085)
Other Devices by Shenzhen Lifotronic Technology Co., Ltd.
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