gudid
Primary ID: IAN 387871_2101
Silvercrest (UDI IAN 387871_2101)
Manufactured by LIDL US, LLC
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Silvercrest - Primary ID IAN 387871_2101
Device Regulatory Overview
The Silvercrest (Model/Catalog Number: IAN 387871_2101) is a medical device manufactured by LIDL US, LLC. This product is indexed under FDA Product Code / Category Classification PGJ within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- IAN 387871_2101
- Product Code / EMDN
- PGJ
- Device Name
- SPO55 Pulse Oximeter intended for wellness use in measuring the blood oxygen saturation and the heart rate (pulse rate).
- Database Sync Date
- 2026-08-09 09:26:08
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 Silvercrest?
The registered manufacturer of record for Silvercrest is LIDL US, LLC.
What is the Primary UDI-DI identifier for Silvercrest?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is IAN 387871_2101.
What classification code is assigned to this device?
This device is registered under product classification code PGJ.
Similar Classification Devices (PGJ)
Other Devices by LIDL US, LLC
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