V-Guide

GUDID 08800142923999

RF Medical Co.,Ltd.

Needle guide, single-use

• Primary Device ID: 08800142923999
• NIH Device Record Key: d461d149-63d7-4a33-af4d-2594c193216f
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: V-Guide
• Version Model Number: VG2004
• Company DUNS: 690514869
• Company Name: RF Medical 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800142923982 [Primary]
GS1	08800142923999 [Package]; Contains: 08800142923982; Package: [10 Units]; In Commercial Distribution
GS1	08800142924002 [Package]; Contains: 08800142923982; Package: [20 Units]; In Commercial Distribution

FDA Product Code

• HDQ: Dilator, Cervical, Fixed Size

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-11-02
• Device Publish Date: 2023-10-25

On-Brand Devices [V-Guide]

• 08800142919374: VG2006S
• 08800142919350: VG2002S
• 08800142919343: VG1606S
• 08800142919329: VG1602S
• 08800142919282: VG2004
• 08800142919275: VG1606
• 08800142919268: VG1604
• 08800142918315: VG1602
• 08800142915352: VG2002
• 08800142914874: VG2006
• 08800142924149: VG2002S
• 08800142924118: VG2006S
• 08800142924088: VG1602S
• 08800142924057: VG1606S
• 08800142924026: VG2002
• 08800142923999: VG2004
• 08800142923920: VG1602
• 08800142923890: VG1604
• 08800142923869: VG1606