GUDIDData
eudamed_udi Primary ID: 05213003192893

ΣΑΚΧΑΡΟ LIQUID 10x50 ml (HIT) (UDI 05213003192893)

Manufactured by Biotechnological Applications Ltd

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for ΣΑΚΧΑΡΟ LIQUID 10x50 ml (HIT) - Primary ID 05213003192893

Device Regulatory Overview

The ΣΑΚΧΑΡΟ LIQUID 10x50 ml (HIT) (Model/Catalog Number: 001734) is a medical device manufactured by Biotechnological Applications Ltd. This product is indexed under FDA Product Code / Category Classification W01010213 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
001734
Product Code / EMDN
W01010213
Device Name
ΣΑΚΧΑΡΟ LIQUID 10x50 ml (HIT)
Database Sync Date
2026-08-09 17:07:21

Full Regulatory Attributes

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

Unlock Compliance Data & Serialization Specs

Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.

Get API Token Access ($49/mo)

Frequently Asked Questions

Who is the primary manufacturer of ΣΑΚΧΑΡΟ LIQUID 10x50 ml (HIT)?

The registered manufacturer of record for ΣΑΚΧΑΡΟ LIQUID 10x50 ml (HIT) is Biotechnological Applications Ltd.

What is the Primary UDI-DI identifier for ΣΑΚΧΑΡΟ LIQUID 10x50 ml (HIT)?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05213003192893.

What classification code is assigned to this device?

This device is registered under product classification code W01010213.

Programmatic Export

Export this master device record as standardized JSON or CSV for compliance audits.

JSON API Endpoint