GUDID 06970784670031

wenzhou dongfang medical instrument co.,ltd

Blood pressure cuff, reusable

• Primary Device ID: 06970784670031
• NIH Device Record Key: 2eaae218-a275-4a74-afd6-108479a7f7e4
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: KT-A05
• Company DUNS: 529870243
• Company Name: wenzhou dongfang medical instrument 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: false
• Lot Batch: true
• Serial Number: false
• 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	06970784670031 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K081951

FDA Product Code

• DXQ: Blood Pressure Cuff

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: 2021-11-30
• Device Publish Date: 2021-11-22

Devices Manufactured by wenzhou dongfang medical instrument co.,ltd

• 06970784670130 - NA: 2024-05-14
• 06970784670147 - NA: 2024-05-14
• 06970784670154 - NA: 2024-05-14
• 06970784670161 - NA: 2024-05-14
• 06970784670123 - NA: 2024-03-22
• 06970784670093 - NA: 2023-12-14
• 06970784670116 - NA: 2023-12-14
• 06970784670048 - N/A: 2022-04-04