ULTRAMED EXTENSION TUBE (High Pressure) - 7 cm (UDI 06223004251658)
Manufactured by Ultra For Medical Products (Ultramed) U.M.I.C (S.A.E)
Device Regulatory Overview
The ULTRAMED EXTENSION TUBE (High Pressure) - 7 cm (Model/Catalog Number: 1011/HP-07) 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 A03020102 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 1011/HP-07
- Product Code / EMDN
- A03020102
- Device Name
- ULTRAMED EXTENSION TUBE
- Database Sync Date
- 2026-08-09 16:30:02
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 EXTENSION TUBE (High Pressure) - 7 cm?
The registered manufacturer of record for ULTRAMED EXTENSION TUBE (High Pressure) - 7 cm is Ultra For Medical Products (Ultramed) U.M.I.C (S.A.E).
What is the Primary UDI-DI identifier for ULTRAMED EXTENSION TUBE (High Pressure) - 7 cm?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 06223004251658.
What classification code is assigned to this device?
This device is registered under product classification code A03020102.
Similar Classification Devices (A03020102)
Other Devices by Ultra For Medical Products (Ultramed) U.M.I.C (S.A.E)
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