GUDIDData
eudamed_udi Primary ID: 15060069283181

Asepsis Universal Aseptic Pack Medium (UDI 15060069283181)

Manufactured by Richardson Healthcare Limited

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Asepsis Universal Aseptic Pack Medium - Primary ID 15060069283181

Device Regulatory Overview

The Asepsis Universal Aseptic Pack Medium (Model/Catalog Number: 958100) is a medical device manufactured by Richardson Healthcare Limited. This product is indexed under FDA Product Code / Category Classification T0203 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
958100
Product Code / EMDN
T0203
Device Name
Asepsis Universal Aseptic Pack Medium
Database Sync Date
2026-08-09 16:49:47

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 Asepsis Universal Aseptic Pack Medium?

The registered manufacturer of record for Asepsis Universal Aseptic Pack Medium is Richardson Healthcare Limited.

What is the Primary UDI-DI identifier for Asepsis Universal Aseptic Pack Medium?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 15060069283181.

What classification code is assigned to this device?

This device is registered under product classification code T0203.

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