HYDROGEN PEROXIDE CARTRIDGES (UDI S900101)
Device Regulatory Overview
The HYDROGEN PEROXIDE CARTRIDGES (Model/Catalog Number: Unspecified) is a medical device manufactured by . This product is indexed under FDA Product Code / Category Classification S900101 within international Unique Device Identification (UDI) compliance databases.
Enforcement actions are currently active for this product line.
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Technical Specifications
- Model Number
- N/A
- Product Code / EMDN
- S900101
- Device Name
- HYDROGEN PEROXIDE CARTRIDGES
- Database Sync Date
- 2026-08-09 16:18:37
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 HYDROGEN PEROXIDE CARTRIDGES?
The registered manufacturer of record for HYDROGEN PEROXIDE CARTRIDGES is .
What is the Primary UDI-DI identifier for HYDROGEN PEROXIDE CARTRIDGES?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is S900101.
What classification code is assigned to this device?
This device is registered under product classification code S900101.
Similar Classification Devices (S900101)
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