eudamed_udi
Primary ID: 08592156097659
LDL C DIRECT 240 (UDI 08592156097659)
Manufactured by Erba Lachema s.r.o.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LDL C DIRECT 240 - Primary ID 08592156097659
Device Regulatory Overview
The LDL C DIRECT 240 (Model/Catalog Number: BLT00042) is a medical device manufactured by Erba Lachema s.r.o.. This product is indexed under FDA Product Code / Category Classification W01010221 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- BLT00042
- Product Code / EMDN
- W01010221
- Device Name
- LDL CHOLESTEROL DIRECT
- Database Sync Date
- 2026-08-09 17:18:34
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 LDL C DIRECT 240?
The registered manufacturer of record for LDL C DIRECT 240 is Erba Lachema s.r.o..
What is the Primary UDI-DI identifier for LDL C DIRECT 240?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08592156097659.
What classification code is assigned to this device?
This device is registered under product classification code W01010221.
Similar Classification Devices (W01010221)
Other Devices by Erba Lachema s.r.o.
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