gudid
Primary ID: K7621
RIDASCREEN Echinococcus IgG (UDI K7621)
Manufactured by R-Biopharm AG
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for RIDASCREEN Echinococcus IgG - Primary ID K7621
Device Regulatory Overview
The RIDASCREEN Echinococcus IgG (Model/Catalog Number: K7621) is a medical device manufactured by R-Biopharm AG. This product is indexed under FDA Product Code / Category Classification within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- K7621
- Product Code / EMDN
- N/A
- Device Name
- The RIDASCREEN Echinococcus IgG test is an enzyme immunoassay for the qualitative determination of IgG antibodies against Echinococcus granulosus und Echinococcus multilocularis in human serum. The test should be used for confirmation purposes when there is a suspected case of infection with Echinococcus.
- Database Sync Date
- 2026-08-09 09:11:27
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of RIDASCREEN Echinococcus IgG?
The registered manufacturer of record for RIDASCREEN Echinococcus IgG is R-Biopharm AG.
What is the Primary UDI-DI identifier for RIDASCREEN Echinococcus IgG?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is K7621.
What classification code is assigned to this device?
This device is registered under product classification code .
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