ULTRAMED ENDOTRACHEAL TUBE Preformed Nasal Uncuffed Size 7 (UDI 06223004254475)
Manufactured by Ultra For Medical Products (Ultramed) U.M.I.C (S.A.E)
Device Regulatory Overview
The ULTRAMED ENDOTRACHEAL TUBE Preformed Nasal Uncuffed Size 7 (Model/Catalog Number: 4010-7/PN) is a medical device manufactured by Ultra For Medical Products (Ultramed) U.M.I.C (S.A.E). This product is indexed under FDA Product Code / Category Classification R01030101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 4010-7/PN
- Product Code / EMDN
- R01030101
- Device Name
- ULTRAMED ENDOTRACHEAL TUBE
- Database Sync Date
- 2026-08-09 16:29:21
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 ULTRAMED ENDOTRACHEAL TUBE Preformed Nasal Uncuffed Size 7?
The registered manufacturer of record for ULTRAMED ENDOTRACHEAL TUBE Preformed Nasal Uncuffed Size 7 is Ultra For Medical Products (Ultramed) U.M.I.C (S.A.E).
What is the Primary UDI-DI identifier for ULTRAMED ENDOTRACHEAL TUBE Preformed Nasal Uncuffed Size 7?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06223004254475.
What classification code is assigned to this device?
This device is registered under product classification code R01030101.
Similar Classification Devices (R01030101)
Other Devices by Ultra For Medical Products (Ultramed) U.M.I.C (S.A.E)
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