eudamed_udi
Primary ID: 08051881027411
MARCUS LT41 (UDI 08051881027411)
Manufactured by CHINESPORT S.P.A.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for MARCUS LT41 - Primary ID 08051881027411
Device Regulatory Overview
The MARCUS LT41 (Model/Catalog Number: LT41ED1060WR) is a medical device manufactured by CHINESPORT S.P.A.. This product is indexed under FDA Product Code / Category Classification V080603 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- LT41ED1060WR
- Product Code / EMDN
- V080603
- Device Name
- MARCUS
- Database Sync Date
- 2026-08-09 16:29:36
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 MARCUS LT41?
The registered manufacturer of record for MARCUS LT41 is CHINESPORT S.P.A..
What is the Primary UDI-DI identifier for MARCUS LT41?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 08051881027411.
What classification code is assigned to this device?
This device is registered under product classification code V080603.
Similar Classification Devices (V080603)
Other Devices by CHINESPORT S.P.A.
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