gudid
Primary ID: 700/7310US
DIMAR (UDI 700/7310US)
Manufactured by HMC PREMEDICAL SPA
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for DIMAR - Primary ID 700/7310US
Device Regulatory Overview
The DIMAR (Model/Catalog Number: 700/7310US) is a medical device manufactured by HMC PREMEDICAL SPA. This product is indexed under FDA Product Code / Category Classification CBK within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- 700/7310US
- Product Code / EMDN
- CBK
- Device Name
- "DIMAX" TOTAL FACE MASK FOR NIV SINGLE USE SIZE M
- Database Sync Date
- 2026-08-09 09:04:28
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 DIMAR?
The registered manufacturer of record for DIMAR is HMC PREMEDICAL SPA.
What is the Primary UDI-DI identifier for DIMAR?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is 700/7310US.
What classification code is assigned to this device?
This device is registered under product classification code CBK.
Similar Classification Devices (CBK)
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