REFAGO

GUDID 06970649350115

Shenzhen Kairuigeli Investment Consultant Co., Ltd.

Foetal Doppler system probe Foetal Doppler system probe Foetal Doppler system probe Foetal Doppler system probe Foetal Doppler system probe Foetal Doppler system probe Foetal Doppler system probe Foetal Doppler system probe Foetal Doppler system probe Foetal Doppler system probe Foetal Doppler system probe Foetal Doppler system probe

• Primary Device ID: 06970649350115
• NIH Device Record Key: 5300bb31-cea9-4d27-8547-7d74bf6ccc48
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: REFAGO
• Version Model Number: 100S
• Company DUNS: 544433016
• Company Name: Shenzhen Kairuigeli Investment Consultant Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• 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	06970649350115 [Primary]

FDA Product Code

• KNG: Monitor, Ultrasonic, Fetal

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2016-12-16

On-Brand Devices [REFAGO]

• 06970649350115: 100S
• 06970649350092: FR-200
• 06970649350085: MT-4320