gudid
Primary ID: V-HTF-P1
V-HEPES PLUS (UDI V-HTF-P1)
Manufactured by VITROMED GmbH
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for V-HEPES PLUS - Primary ID V-HTF-P1
Device Regulatory Overview
The V-HEPES PLUS (Model/Catalog Number: V-HTF-P1) is a medical device manufactured by VITROMED GmbH. This product is indexed under FDA Product Code / Category Classification MQL within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- V-HTF-P1
- Product Code / EMDN
- MQL
- Device Name
- V-HEPES PLUS is intended for oocyte collection, intracytoplasmic sperm injection (ICSI) fertilization, and oocyte and embryo washing and handling procedures. V-HEPES PLUS is also intended for transfer of embryos to the uterine cavity.
- Database Sync Date
- 2026-08-09 09:53:17
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 V-HEPES PLUS?
The registered manufacturer of record for V-HEPES PLUS is VITROMED GmbH.
What is the Primary UDI-DI identifier for V-HEPES PLUS?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is V-HTF-P1.
What classification code is assigned to this device?
This device is registered under product classification code MQL.
Similar Classification Devices (MQL)
Other Devices by VITROMED GmbH
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