iChoice

GUDID 00846841019562

iChoice Fingtertip Pulse Oximeter OX200

Beijing Choice Electronic Technology Co., Ltd.

Pulse oximeter, battery-powered

• Primary Device ID: 00846841019562
• NIH Device Record Key: 22138149-148b-4db2-92fd-221a657f6e9c
• 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	00846841019562 [Primary]
GS1	10846841019569 [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: 2020-05-04
• Device Publish Date: 2020-04-24

On-Brand Devices [iChoice]

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