Spacelabs

GUDID 06946725527993

6946725527993

APK Technology Co.,Ltd.

Electrocardiographic lead set, reusable

• Primary Device ID: 06946725527993
• NIH Device Record Key: 651509e6-9de1-413c-a3d7-fd5501fdaa81
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Spacelabs
• Version Model Number: A1902-C02
• 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: 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	06946725527993 [Primary]

FDA Product Code

• IKD: Cable, Electrode

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: 2020-08-27
• Device Publish Date: 2020-08-19

On-Brand Devices [Spacelabs]

• 06946725527306: A0006D05-001
• 06946725527290: A0006D05
• 06946725527283: A0006D03-001
• 06946725527276: A0006D03
• 06946725527993: 6946725527993
• 06946725529027: Spacelabs Ultra-Philips 5L ECG Adapter
• 06946725529010: Spacelabs Ultra-Philips 3L ECG Adapter