VitaVitro

GUDID 06971982050502

SHENZHEN VITAVITRO BIOTECH CO.,LTD.

Assisted reproduction microtool

• Primary Device ID: 06971982050502
• NIH Device Record Key: d0cd8f56-f081-418a-b723-6d5084be1ac5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: VitaVitro
• Version Model Number: Micromanipulation Pipettes, Biopsy Pipette
• Company DUNS: 544504573
• Company Name: SHENZHEN VITAVITRO BIOTECH CO.,LTD.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: true
• MRI Safety Status: Labeling does not contain MRI Safety Information
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06971982050502 [Primary]

FDA Product Code

• PUC: Microtools, Assisted Reproduction (Pipettes), Exempt

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2025-02-19
• Device Publish Date: 2022-12-22

On-Brand Devices [VitaVitro]

• 06971982050519: Micromanipulation Pipettes, Denuding Pipette
• 06971982050502: Micromanipulation Pipettes, Biopsy Pipette
• 06971982050496: Micromanipulation Pipettes, Holding Pipette
• 06971982050489: Micromanipulation Pipettes, ICSI Pipette
• 06971982050410: Culture Oil, Oil-1.0,500 ml
• 06971982050403: Culture Oil, Oil-1.0,125ml
• 06971982050397: Culture Oil, Oil-1.0, 60ml