Skanray

GUDID 10840935110477

SUNTECH MEDICAL, INC.

Blood pressure cuff, reusable

• Primary Device ID: 10840935110477
• NIH Device Record Key: e69bd5bf-3ad5-4c8b-98c3-a493462e3135
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Skanray
• Version Model Number: 98-0606-08
• Company DUNS: 148191133
• Company Name: SUNTECH MEDICAL, INC.
• 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

Customer Support Contacts

• Phone: +1-919-654-2300
• Email: UDI_mail@suntechmed.com
• Phone: +1-919-654-2300
• Email: UDI_mail@suntechmed.com
• Phone: +1-919-654-2300
• Email: UDI_mail@suntechmed.com
• Phone: +1-919-654-2300
• Email: UDI_mail@suntechmed.com
• Phone: +1-919-654-2300
• Email: UDI_mail@suntechmed.com
• Phone: +1-919-654-2300
• Email: UDI_mail@suntechmed.com
• Phone: +1-919-654-2300
• Email: UDI_mail@suntechmed.com
• Phone: +1-919-654-2300
• Email: UDI_mail@suntechmed.com
• Phone: +1-919-654-2300
• Email: UDI_mail@suntechmed.com
• Phone: +1-919-654-2300
• Email: UDI_mail@suntechmed.com
• Phone: +1-919-654-2300
• Email: UDI_mail@suntechmed.com
• Phone: +1-919-654-2300
• Email: UDI_mail@suntechmed.com
• Phone: +1-919-654-2300
• Email: UDI_mail@suntechmed.com
• Phone: +1-919-654-2300
• Email: UDI_mail@suntechmed.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10840935110477 [Primary]

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: 2024-06-28
• Device Publish Date: 2024-06-20

Devices Manufactured by SUNTECH MEDICAL, INC.

• 10840935110477 - Skanray: 2024-06-28
• 10840935110477 - Skanray: 2024-06-28
• 10840935110217 - ProLife: 2023-06-19
• 10840935110224 - SunTech APC: 2023-06-19
• 10840935110231 - ProLife: 2023-06-19
• 10840935110248 - ProLife: 2023-06-19
• 10840935110255 - ProLife: 2023-06-19
• 10840935110262 - ProLife: 2023-06-19
• 10840935110279 - SunTech APC: 2023-06-19