Axiom Dual-Sump Atraum With ClotStop (UDI 111196ATSR)
Manufactured by AXIOM MEDICAL, INCORPORATED
Device Regulatory Overview
The Axiom Dual-Sump Atraum With ClotStop (Model/Catalog Number: 111196ATSR) is a medical device manufactured by AXIOM MEDICAL, INCORPORATED. This product is indexed under FDA Product Code / Category Classification GBS within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 111196ATSR
- Product Code / EMDN
- GBS
- Device Name
- Sump Drain, Three Lumens, Silicone, Small Eye, With Suture Ring, With ClotStop
- Database Sync Date
- 2026-08-09 09:36:12
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 Axiom Dual-Sump Atraum With ClotStop?
The registered manufacturer of record for Axiom Dual-Sump Atraum With ClotStop is AXIOM MEDICAL, INCORPORATED.
What is the Primary UDI-DI identifier for Axiom Dual-Sump Atraum With ClotStop?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 111196ATSR.
What classification code is assigned to this device?
This device is registered under product classification code GBS.
Similar Classification Devices (GBS)
Other Devices by AXIOM MEDICAL, INCORPORATED
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