eudamed_udi
Primary ID: 06970701961938
lifesense (UDI 06970701961938)
Manufactured by Taian Dalu Medical Instrument Co., Ltd.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for lifesense - Primary ID 06970701961938
Device Regulatory Overview
The lifesense (Model/Catalog Number: MD1012) is a medical device manufactured by Taian Dalu Medical Instrument Co., Ltd.. This product is indexed under FDA Product Code / Category Classification R9001 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- MD1012
- Product Code / EMDN
- R9001
- Device Name
- Medical Mouthpieces
- Database Sync Date
- 2026-08-09 17:25:18
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 lifesense?
The registered manufacturer of record for lifesense is Taian Dalu Medical Instrument Co., Ltd..
What is the Primary UDI-DI identifier for lifesense?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06970701961938.
What classification code is assigned to this device?
This device is registered under product classification code R9001.
Similar Classification Devices (R9001)
Other Devices by Taian Dalu Medical Instrument Co., Ltd.
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