gudid
Primary ID: R30368601
Streptex Disposable Reaction Cards RT02 (UDI R30368601)
Manufactured by REMEL EUROPE LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Streptex Disposable Reaction Cards RT02 - Primary ID R30368601
Device Regulatory Overview
The Streptex Disposable Reaction Cards RT02 (Model/Catalog Number: R30368601) is a medical device manufactured by REMEL EUROPE LIMITED. This product is indexed under FDA Product Code / Category Classification JTO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- R30368601
- Product Code / EMDN
- JTO
- Device Name
- Database Sync Date
- 2026-08-09 09:08:12
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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Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of Streptex Disposable Reaction Cards RT02?
The registered manufacturer of record for Streptex Disposable Reaction Cards RT02 is REMEL EUROPE LIMITED.
What is the Primary UDI-DI identifier for Streptex Disposable Reaction Cards RT02?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is R30368601.
What classification code is assigned to this device?
This device is registered under product classification code JTO.
Similar Classification Devices (JTO)
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