gudid
Primary ID: R30951001
Streptex Extraction Enzyme (UDI R30951001)
Manufactured by REMEL EUROPE LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for Streptex Extraction Enzyme - Primary ID R30951001
Device Regulatory Overview
The Streptex Extraction Enzyme (Model/Catalog Number: R30951001) 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
- R30951001
- 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 Extraction Enzyme?
The registered manufacturer of record for Streptex Extraction Enzyme is REMEL EUROPE LIMITED.
What is the Primary UDI-DI identifier for Streptex Extraction Enzyme?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is R30951001.
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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