Fingertip Pluse Oximeter

GUDID 06932562310355

Guangdong Biolight Meditech Co., Ltd.

Pulse oximeter

• Primary Device ID: 06932562310355
• NIH Device Record Key: b47aaacf-4e2b-4bb8-90ec-349d72045548
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Fingertip Pluse Oximeter
• Version Model Number: M70D
• Company DUNS: 530120146
• Company Name: Guangdong Biolight Meditech Co., Ltd.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• 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: false
• 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	06932562310355 [Primary]

FDA Product Code

• DQA: Oximeter

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: 2024-04-08
• Device Publish Date: 2024-03-29

On-Brand Devices [Fingertip Pluse Oximeter]

• 06932562310256: M70B
• 06932562310027: M70C
• 06932562310010: M70A
• 06932562310355: M70D