DOPPLER MODEL 1059-C W/PPG

GUDID 00816787020069

PARKS MEDICAL ELECTRONICS, INC.

Limb plethysmograph Limb plethysmograph Limb plethysmograph

• Primary Device ID: 00816787020069
• NIH Device Record Key: 6f29beae-b454-4157-b3b6-f8701c36b256
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DOPPLER MODEL 1059-C W/PPG
• Version Model Number: 1059-C
• Company DUNS: 009041773
• Company Name: PARKS MEDICAL ELECTRONICS, INC.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: true
• 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: true
• 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

Customer Support Contacts

• Phone: +1(800)547-6427
• Email: twelker@parksmed.com
• Phone: +1(800)547-6427
• Email: twelker@parksmed.com
• Phone: +1(800)547-6427
• Email: twelker@parksmed.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00816787020069 [Primary]

FDA Product Code

• JOM: PLETHYSMOGRAPH, PHOTOELECTRIC, PNEUMATIC OR HYDRAULIC

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: 2018-03-29
• Device Publish Date: 2016-09-24

On-Brand Devices [DOPPLER MODEL 1059-C W/PPG]

• 00816787020076: 1059-C(F)
• 00816787020069: 1059-C