eudamed_udi Primary ID: 05213003193135

CRP LATEX R1:1x40, R2:1x10ml (BS200) (UDI 05213003193135)

Manufactured by Biotechnological Applications Ltd

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

Scannable UDI-DI Representation

Device Regulatory Overview

The CRP LATEX R1:1x40, R2:1x10ml (BS200) (Model/Catalog Number: 001832) is a medical device manufactured by Biotechnological Applications Ltd. This product is indexed under FDA Product Code / Category Classification W01021109 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: 001832
Product Code / EMDN: W01021109
Device Name: CRP LATEX R1:1x40, R2:1x10ml (BS200)
Database Sync Date: 2026-08-09 17:02:33

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 CRP LATEX R1:1x40, R2:1x10ml (BS200)?

The registered manufacturer of record for CRP LATEX R1:1x40, R2:1x10ml (BS200) is Biotechnological Applications Ltd.

What is the Primary UDI-DI identifier for CRP LATEX R1:1x40, R2:1x10ml (BS200)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05213003193135.

What classification code is assigned to this device?

This device is registered under product classification code W01021109.

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