Mindray

GUDID 06946725529041

Mindray Bene/Pass-Philips 5L ECG Adapter

APK Technology Co.,Ltd.

Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable Electrocardiographic lead set, reusable

• Primary Device ID: 06946725529041
• NIH Device Record Key: 557ef0f9-4733-450c-86a5-afd3897df8cb
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Mindray
• Version Model Number: A-CO-183
• Company DUNS: 529691989
• Company Name: APK 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: true
• Donation Id Number: true
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	06946725529041 [Primary]
GS1	16946725590642 [Package]; Package: [25 Units]; In Commercial Distribution
GS1	16946725590925 [Package]; Package: [200 Units]; In Commercial Distribution

FDA Product Code

• IKD: Cable, Electrode

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 2
• Public Version Date: 2021-09-01
• Device Publish Date: 2021-05-28

On-Brand Devices [Mindray]

• 06946725520703: A1318-SW111PU
• 06946725520697: A1318-SP111PU
• 06946725520680: A1318-SP111PV
• 06946725520673: A1318-SA111PU
• 06946725520666: A1318-SA111PV
• 06946725520642: A0509-SW111PU
• 06946725520635: A0509-SP111PU
• 06946725520628: A0509-SP111PV
• 06946725520611: A0509-SA111PU
• 06946725520604: A0509-SA111PV
• 06946725520581: A1318-SW129PU
• 06946725520574: A1318-SP129PU
• 06946725520567: A1318-SP129PV
• 06946725520550: A1318-SA129PU
• 06946725520543: A1318-SA129PV
• 06946725528631: MDR-009-004782-00-DP
• 06946725528624: MDR-009-004786-00-DP
• 06946725528617: MDR-009-004782-00
• 06946725528600: MDR-009-004786-00
• 06946725529041: Mindray Bene/Pass-Philips 5L ECG Adapter
• 06946725529034: Mindray Pano-Philips 3L ECG Adapter
• 06946725528686: MDR-009-004782-00
• 06946725528679: MDR-009-004786-00