Moving-Shot Guide

GUDID 08800142915079

RF Medical Co.,Ltd.

Nonimplantable needle guide, single-use

• Primary Device ID: 08800142915079
• NIH Device Record Key: 301d552c-28eb-4cea-93ee-265effbb38c8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Moving-Shot Guide
• Version Model Number: NGL18-A2-L3-12H
• 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: false
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: true
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	08800142915079 [Primary]

FDA Product Code

• OIJ: Biopsy Needle Guide Kit

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-01-20
• Device Publish Date: 2022-01-12

On-Brand Devices [Moving-Shot Guide]

• 08809295149966: Needle guide
• 08800142915079: NGL18-A2-L3-12H