GUDIDData
eudamed_udi Primary ID: D-DED-R1025L

EDDP Rapid Test Cassette (UDI D-DED-R1025L)

Manufactured by Hangzhou Alltest Biotech.Co.,Ltd.

Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for EDDP Rapid Test Cassette - Primary ID D-DED-R1025L

Device Regulatory Overview

The EDDP Rapid Test Cassette (Model/Catalog Number: DED-R102) is a medical device manufactured by Hangzhou Alltest Biotech.Co.,Ltd.. This product is indexed under FDA Product Code / Category Classification W0102160507 within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number
DED-R102
Product Code / EMDN
W0102160507
Device Name
EDDP Rapid Test Cassette
Database Sync Date
2026-08-09 16:29:23

Full Regulatory Attributes

πŸ”’ 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 EDDP Rapid Test Cassette?

The registered manufacturer of record for EDDP Rapid Test Cassette is Hangzhou Alltest Biotech.Co.,Ltd..

What is the Primary UDI-DI identifier for EDDP Rapid Test Cassette?

The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is D-DED-R1025L.

What classification code is assigned to this device?

This device is registered under product classification code W0102160507.

Programmatic Export

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

JSON API Endpoint