kingst

GUDID 06974774500032

Beijing Kingst Commercial & Trade Co., Ltd.

Pulse oximeter

• Primary Device ID: 06974774500032
• NIH Device Record Key: 38d0258a-48da-46f0-9d69-d9035b507e66
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: kingst
• Version Model Number: Capno-H
• Company DUNS: 527224872
• Company Name: Beijing Kingst Commercial & Trade 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: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: true
• 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	06974774500032 [Primary]

FDA Product Code

• CCK: Analyzer, Gas, Carbon-Dioxide, Gaseous-Phase

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: 2025-01-23
• Device Publish Date: 2025-01-15