eudamed_udi
Primary ID: 00816085024097
NALC Diluent (UDI 00816085024097)
Manufactured by CalibreScientific US, Inc.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for NALC Diluent - Primary ID 00816085024097
Device Regulatory Overview
The NALC Diluent (Model/Catalog Number: 0004820) is a medical device manufactured by CalibreScientific US, Inc.. This product is indexed under FDA Product Code / Category Classification W010499 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 0004820
- Product Code / EMDN
- W010499
- Device Name
- Digestion and Decontamination Reagents
- Database Sync Date
- 2026-08-09 17:33:24
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 NALC Diluent?
The registered manufacturer of record for NALC Diluent is CalibreScientific US, Inc..
What is the Primary UDI-DI identifier for NALC Diluent?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00816085024097.
What classification code is assigned to this device?
This device is registered under product classification code W010499.
Similar Classification Devices (W010499)
Other Devices by CalibreScientific US, Inc.
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