RENONMED

GUDID 06975976450064

Zhejiang Renon Medical Instrument Co., Ltd.

Oral/upper respiratory tract specimen collection swab

• Primary Device ID: 06975976450064
• NIH Device Record Key: 6bf819eb-5573-4341-be90-d5686bf14975
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: RENONMED
• Version Model Number: NS
• Company DUNS: 553185520
• Company Name: Zhejiang Renon Medical Instrument 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: true
• 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	06975976450064 [Primary]

FDA Product Code

• KXG: Applicator, Absorbent Tipped, Sterile

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: 2023-02-24
• Device Publish Date: 2023-02-16

On-Brand Devices [RENONMED]

• 06975976450064: NS
• 06975976450057: 005
• 06975976450040: 004
• 06975976450033: 003
• 06975976450026: 002
• 06975976450019: 001
• 06975976450149: 014
• 06975976450132: 013
• 06975976450125: 012
• 06975976450118: 011
• 06975976450101: 010
• 06975976450095: 009
• 06975976450088: 008
• 06975976450071: 007