eudamed_udi Primary ID: 05213003192336

LDL-D R1:1x30 R2:1x10ml (BS-300/380) (UDI 05213003192336)

Manufactured by Biotechnological Applications Ltd

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The LDL-D R1:1x30 R2:1x10ml (BS-300/380) (Model/Catalog Number: 001661) is a medical device manufactured by Biotechnological Applications Ltd. This product is indexed under FDA Product Code / Category Classification W01010221 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 001661
Product Code / EMDN: W01010221
Device Name: LDL-D R1:1x30 R2:1x10ml (BS-300/380)
Database Sync Date: 2026-08-09 17:41:00

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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Frequently Asked Questions

Who is the primary manufacturer of LDL-D R1:1x30 R2:1x10ml (BS-300/380)?

The registered manufacturer of record for LDL-D R1:1x30 R2:1x10ml (BS-300/380) is Biotechnological Applications Ltd.

What is the Primary UDI-DI identifier for LDL-D R1:1x30 R2:1x10ml (BS-300/380)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05213003192336.

What classification code is assigned to this device?

This device is registered under product classification code W01010221.

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