Unspecified Brand (UDI 04049051076707)
Manufactured by Intensiv Medical Products IMPROMEDIFORM GmbH
Device Regulatory Overview
The Unspecified Brand (Model/Catalog Number: M18038) is a medical device manufactured by Intensiv Medical Products IMPROMEDIFORM GmbH. This product is indexed under FDA Product Code / Category Classification A03020101 within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- M18038
- Product Code / EMDN
- A03020101
- Device Name
- M01071
- Database Sync Date
- 2026-08-09 16:29:00
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 Unspecified Brand?
The registered manufacturer of record for Unspecified Brand is Intensiv Medical Products IMPROMEDIFORM GmbH.
What is the Primary UDI-DI identifier for Unspecified Brand?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 04049051076707.
What classification code is assigned to this device?
This device is registered under product classification code A03020101.
Similar Classification Devices (A03020101)
Other Devices by Intensiv Medical Products IMPROMEDIFORM GmbH
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