gudid
Primary ID: R21924
REMEL (UDI R21924)
Manufactured by REMEL, INC.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for REMEL - Primary ID R21924
Device Regulatory Overview
The REMEL (Model/Catalog Number: R21924) is a medical device manufactured by REMEL, INC.. This product is indexed under FDA Product Code / Category Classification LIO within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- R21924
- Product Code / EMDN
- LIO
- Device Name
- PVA Modified (15ml Vial) PK/120
- Database Sync Date
- 2026-08-09 09:35:51
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 REMEL?
The registered manufacturer of record for REMEL is REMEL, INC..
What is the Primary UDI-DI identifier for REMEL?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is R21924.
What classification code is assigned to this device?
This device is registered under product classification code LIO.
Similar Classification Devices (LIO)
Other Devices by REMEL, INC.
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