gudid
Primary ID: R30163601
NA (UDI R30163601)
Manufactured by REMEL EUROPE LIMITED
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NA - Primary ID R30163601
Device Regulatory Overview
The NA (Model/Catalog Number: R30163601) is a medical device manufactured by REMEL EUROPE LIMITED. This product is indexed under FDA Product Code / Category Classification GRM within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- R30163601
- Product Code / EMDN
- GRM
- 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 NA?
The registered manufacturer of record for NA is REMEL EUROPE LIMITED.
What is the Primary UDI-DI identifier for NA?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is R30163601.
What classification code is assigned to this device?
This device is registered under product classification code GRM.
Similar Classification Devices (GRM)
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