Atlas RF Latex Kit, 125 Tests (5 ml Latex, 2x1 ml controls, Glass slide, Stirring sticks). (UDI 04260658557943)
Manufactured by Atlas Medical GmbH
Device Regulatory Overview
The Atlas RF Latex Kit, 125 Tests (5 ml Latex, 2x1 ml controls, Glass slide, Stirring sticks). (Model/Catalog Number: 8.00.04.3.0125) is a medical device manufactured by Atlas Medical GmbH. This product is indexed under FDA Product Code / Category Classification W01021110 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 8.00.04.3.0125
- Product Code / EMDN
- W01021110
- Device Name
- Atlas RF Latex Kit, 125 Tests (5 ml Latex, 2x1 ml controls, Glass slide, Stirring sticks).
- Database Sync Date
- 2026-08-09 16:44:59
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 Atlas RF Latex Kit, 125 Tests (5 ml Latex, 2x1 ml controls, Glass slide, Stirring sticks).?
The registered manufacturer of record for Atlas RF Latex Kit, 125 Tests (5 ml Latex, 2x1 ml controls, Glass slide, Stirring sticks). is Atlas Medical GmbH.
What is the Primary UDI-DI identifier for Atlas RF Latex Kit, 125 Tests (5 ml Latex, 2x1 ml controls, Glass slide, Stirring sticks).?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04260658557943.
What classification code is assigned to this device?
This device is registered under product classification code W01021110.
Similar Classification Devices (W01021110)
Other Devices by Atlas Medical GmbH
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