BERRY®贝瑞

GUDID 06924054330088

SHANGHAI BERRY ELECTRONIC TECH CO., LTD.

Pulse oximeter, battery-powered

• Primary Device ID: 06924054330088
• NIH Device Record Key: da4f53f4-3cb4-4a53-92c9-b436f1fbea46
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: BERRY®贝瑞
• Version Model Number: BM1000
• Company DUNS: 529404533
• Company Name: SHANGHAI BERRY ELECTRONIC TECH 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: true
• Device Combination Product: false
• Single Use: false
• Lot Batch: false
• Serial Number: true
• Manufacturing Date: false
• 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	06924054330088 [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: 2018-06-08
• Device Publish Date: 2018-05-08

On-Brand Devices [BERRY®贝瑞]

• 06924054330088: BM1000
• 06924054330026: BM1000C
• 06924054330002: BM1000A
• 06924054320003: BM2000A