Replacement inductive effort sensor (RIP) (UDI 04250413409198)
Manufactured by SOMNOmedics AG
Device Regulatory Overview
The Replacement inductive effort sensor (RIP) (Model/Catalog Number: TOS080-B) is a medical device manufactured by SOMNOmedics AG. This product is indexed under FDA Product Code / Category Classification Z1203020280 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- TOS080-B
- Product Code / EMDN
- Z1203020280
- Device Name
- Inductiv effort belt
- Database Sync Date
- 2026-08-09 16:30:40
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 Replacement inductive effort sensor (RIP)?
The registered manufacturer of record for Replacement inductive effort sensor (RIP) is SOMNOmedics AG.
What is the Primary UDI-DI identifier for Replacement inductive effort sensor (RIP)?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04250413409198.
What classification code is assigned to this device?
This device is registered under product classification code Z1203020280.
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