gudid
Primary ID: ET-I
VitaVitro (UDI ET-I)
Manufactured by SHENZHEN VITAVITRO BIOTECH CO.,LTD.
Data verified against official FDA/EUDAMED records on
Scannable UDI-DI Representation
GS1-128 UDI Barcode representation for VitaVitro - Primary ID ET-I
Device Regulatory Overview
The VitaVitro (Model/Catalog Number: ET-I) is a medical device manufactured by SHENZHEN VITAVITRO BIOTECH CO.,LTD.. This product is indexed under FDA Product Code / Category Classification MQF within international Unique Device Identification (UDI) compliance databases.
Technical Specifications
- Model Number
- ET-I
- Product Code / EMDN
- MQF
- Device Name
- Database Sync Date
- 2026-08-09 09:06:41
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 VitaVitro?
The registered manufacturer of record for VitaVitro is SHENZHEN VITAVITRO BIOTECH CO.,LTD..
What is the Primary UDI-DI identifier for VitaVitro?
The Primary UDI-DI identifier registered in FDA GUDID and EUDAMED records is ET-I.
What classification code is assigned to this device?
This device is registered under product classification code MQF.
Similar Classification Devices (MQF)
Other Devices by SHENZHEN VITAVITRO BIOTECH CO.,LTD.
Programmatic Export
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