gudid
Primary ID: R40181
REMEL (UDI R40181)
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 R40181
Device Regulatory Overview
The REMEL (Model/Catalog Number: R40181) is a medical device manufactured by REMEL, INC.. This product is indexed under FDA Product Code / Category Classification LIB within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- R40181
- Product Code / EMDN
- LIB
- Device Name
- Acridine Orange, Phenolic Decol BTL/250ml
- 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 R40181.
What classification code is assigned to this device?
This device is registered under product classification code LIB.
Similar Classification Devices (LIB)
Other Devices by REMEL, INC.
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