gudid Primary ID: Micromanipulation Pipettes, ICSI Pipette

VitaVitro (UDI Micromanipulation Pipettes, ICSI Pipette)

Manufactured by SHENZHEN VITAVITRO BIOTECH CO.,LTD.

Data verified against official FDA/EUDAMED records on August 9, 2026

Scannable UDI-DI Representation

Device Regulatory Overview

The VitaVitro (Model/Catalog Number: Micromanipulation Pipettes, ICSI Pipette) is a medical device manufactured by SHENZHEN VITAVITRO BIOTECH CO.,LTD.. This product is indexed under FDA Product Code / Category Classification PUC within international Unique Device Identification (UDI) compliance databases.

Technical Specifications

Model Number: Micromanipulation Pipettes, ICSI Pipette
Product Code / EMDN: PUC
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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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 Micromanipulation Pipettes, ICSI Pipette.

What classification code is assigned to this device?

This device is registered under product classification code PUC.

Similar Classification Devices (PUC)

Other Devices by SHENZHEN VITAVITRO BIOTECH CO.,LTD.

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