iChoice

GUDID 00846841019371

iChoice OX200 Smart pulse oximeter

Beijing Choice Electronic Technology Co., Ltd.

Pulse oximeter, battery-powered Pulse oximeter, battery-powered Pulse oximeter, battery-powered Pulse oximeter, battery-powered Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter Pulse oximeter

• Primary Device ID: 00846841019371
• NIH Device Record Key: 40884546-5013-4a59-a852-1b6c9e0816d2
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: iChoice
• Version Model Number: OX200
• Company DUNS: 526882823
• Company Name: Beijing Choice Electronic Technology 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: false
• Lot Batch: false
• Serial Number: true
• 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	00846841019371 [Primary]
GS1	10846841019378 [Package]; Package: [48 Units]; In Commercial Distribution

FDA Product Code

• PGJ: Oximeter, Wellness

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: 2019-03-28
• Device Publish Date: 2019-03-20

On-Brand Devices [iChoice]

• 00846841019371: iChoice OX200 Smart pulse oximeter
• 00846841070921: iChoice Fingtertip Pulse Oximeter OX200
• 00846841019562: iChoice Fingtertip Pulse Oximeter OX200