GUDIDData
eudamed_udi Primary ID: 06933289810371

Finecare (UDI 06933289810371)

Manufactured by Guangzhou Wondfo Biotech Co., Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Finecare - Primary ID 06933289810371

Device Regulatory Overview

The Finecare (Model/Catalog Number: W242) is a medical device manufactured by Guangzhou Wondfo Biotech Co., Ltd.. This product is indexed under FDA Product Code / Category Classification W01021312 within international Unique Device Identification (UDI) compliance databases.

ACTIVE SAFETY RECALL ALERT 3 Event(s) Found

Enforcement actions are currently active for this product line.

ID: Z-2787-2018 View Full Alert →

TCube One Step Multi-Drug Oral Fluid Test Cube (AMPSO,COC20,METSO, OPl40,OXY20,THC2S) Product Usage: T-Cube One Step Multi-Drug Oral Flu...

πŸ”’ Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-2788-2018 View Full Alert →

TCube One Step Multi-Drug Oral Fluid Test Cube (AMPSO, BARGO, BZ030,COC20,MDMA100,METSO, MTD30,OPl40,OXY20, THC2S) Product Usage: T-Cube...

πŸ”’ Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)
ID: Z-2789-2018 View Full Alert →

TCube One Step Multi-Drug Oral Fluid Test Cube (AMPSO, BARGO, SUPS, BZ030, COC20,MDMAlOO, METSO, OPl40,OXY20,THC2S) Product Usage: T-Cu...

πŸ”’ Compromised Lot & Serial Numbers Locked
Verify if facility inventory is affected by this recall.
Unlock Lot Data ($49)

Technical Specifications

Model Number
W242
Product Code / EMDN
W01021312
Device Name
Finecareβ„’ Lp-PLA2 Rapid Quantitative Test
Database Sync Date
2026-08-09 16:29:09

Full Regulatory Attributes

πŸ”’ Token Gated
{
    "review_panel": "AN",
    "gudid_di_status": "Published",
    "sterilization_methods": ["EO", "Gamma"],
    "rx_only": true
}
                            

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Frequently Asked Questions

Who is the primary manufacturer of Finecare?

The registered manufacturer of record for Finecare is Guangzhou Wondfo Biotech Co., Ltd..

What is the Primary UDI-DI identifier for Finecare?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06933289810371.

What classification code is assigned to this device?

This device is registered under product classification code W01021312.

Similar Classification Devices (W01021312)

Other Devices by Guangzhou Wondfo Biotech Co., Ltd.

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