REFAGO

GUDID 06970649350115

Shenzhen Kairuigeli Investment Consultant Co., Ltd.

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