Duo-Check Heat Sealing Sterilization Pouches (UDI 10732224109968)
Manufactured by Crosstex International Inc
Device Regulatory Overview
The Duo-Check Heat Sealing Sterilization Pouches (Model/Catalog Number: SC1015HS) is a medical device manufactured by Crosstex International Inc. This product is indexed under FDA Product Code / Category Classification S01010101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- SC1015HS
- Product Code / EMDN
- S01010101
- Device Name
- Sterilization Packaging
- Database Sync Date
- 2026-08-09 16:29:33
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 Duo-Check Heat Sealing Sterilization Pouches?
The registered manufacturer of record for Duo-Check Heat Sealing Sterilization Pouches is Crosstex International Inc.
What is the Primary UDI-DI identifier for Duo-Check Heat Sealing Sterilization Pouches?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 10732224109968.
What classification code is assigned to this device?
This device is registered under product classification code S01010101.
Similar Classification Devices (S01010101)
Other Devices by Crosstex International Inc
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