Mucus Extractor (UDI 05033241021904)
Manufactured by Ivor Shaw Ltd trading as Pennine Healthcare
Device Regulatory Overview
The Mucus Extractor (Model/Catalog Number: ME-9112) is a medical device manufactured by Ivor Shaw Ltd trading as Pennine Healthcare. This product is indexed under FDA Product Code / Category Classification R05010301 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ME-9112
- Product Code / EMDN
- R05010301
- Device Name
- Mucus Extractors and Mucus Specimen Traps
- Database Sync Date
- 2026-08-09 16:46:45
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 Mucus Extractor?
The registered manufacturer of record for Mucus Extractor is Ivor Shaw Ltd trading as Pennine Healthcare.
What is the Primary UDI-DI identifier for Mucus Extractor?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 05033241021904.
What classification code is assigned to this device?
This device is registered under product classification code R05010301.
Similar Classification Devices (R05010301)
Other Devices by Ivor Shaw Ltd trading as Pennine Healthcare
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