MUCOSOL™ (Cleland's Reagent) (UDI 00816085023403)
Manufactured by CalibreScientific US, Inc.
Device Regulatory Overview
The MUCOSOL™ (Cleland's Reagent) (Model/Catalog Number: 0003510) 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
- 0003510
- Product Code / EMDN
- W010499
- Device Name
- Digestion and Decontamination Reagents
- Database Sync Date
- 2026-08-09 16:51:21
Full Regulatory Attributes
🔒 Token Gated
{
"review_panel": "AN",
"gudid_di_status": "Published",
"sterilization_methods": ["EO", "Gamma"],
"rx_only": true
}
Unlock Compliance Data & Serialization Specs
Access raw JSON payloads, UDI-DI packaging hierarchies, and Notified Body IDs.
Get API Token Access ($49/mo)Frequently Asked Questions
Who is the primary manufacturer of MUCOSOL™ (Cleland's Reagent)?
The registered manufacturer of record for MUCOSOL™ (Cleland's Reagent) is CalibreScientific US, Inc..
What is the Primary UDI-DI identifier for MUCOSOL™ (Cleland's Reagent)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 00816085023403.
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.
Programmatic Export
Export this master device record as standardized JSON or CSV for compliance audits.
JSON API Endpoint