GUDIDData
eudamed_udi Primary ID: 05213003194354

LDH IFCC-SL R1:6x20, R2:2x15 ml (HIT) (UDI 05213003194354)

Manufactured by Biotechnological Applications Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for LDH IFCC-SL R1:6x20, R2:2x15 ml (HIT) - Primary ID 05213003194354

Device Regulatory Overview

The LDH IFCC-SL R1:6x20, R2:2x15 ml (HIT) (Model/Catalog Number: 001998) is a medical device manufactured by Biotechnological Applications Ltd. This product is indexed under FDA Product Code / Category Classification W01010119 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
001998
Product Code / EMDN
W01010119
Device Name
LDH IFCC-SL R1:6x20, R2:2x15 ml (HIT)
Database Sync Date
2026-08-09 17:18:04

Full Regulatory Attributes

🔒 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 LDH IFCC-SL R1:6x20, R2:2x15 ml (HIT)?

The registered manufacturer of record for LDH IFCC-SL R1:6x20, R2:2x15 ml (HIT) is Biotechnological Applications Ltd.

What is the Primary UDI-DI identifier for LDH IFCC-SL R1:6x20, R2:2x15 ml (HIT)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05213003194354.

What classification code is assigned to this device?

This device is registered under product classification code W01010119.

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