FEATHERLITE AQUA VA00219

GUDID B249VA002191

SUBMERSIBLE TOCODYNAMOMETER TRANSDUCER

PARKER-HANNIFIN CORPORATION

Cardiotocograph transducer Cardiotocograph transducer Tocodynamometer probe Tocodynamometer probe Tocodynamometer probe Tocodynamometer probe Tocodynamometer probe Tocodynamometer probe Tocodynamometer probe Tocodynamometer probe Tocodynamometer probe Tocodynamometer probe Tocodynamometer probe

• Primary Device ID: B249VA002191
• NIH Device Record Key: 59231ef1-515c-4c0d-b5d7-055aaf2c3e7e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: FEATHERLITE AQUA
• Version Model Number: TDW-NB
• Catalog Number: VA00219
• Company DUNS: 008370645
• Company Name: PARKER-HANNIFIN CORPORATION
• Device Count: 25
• 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: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• 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: 805-658-2984
• Email: GEORGENE.AUSTRIA@PARKER.COM
• Phone: 805-658-2984
• Email: GEORGENE.AUSTRIA@PARKER.COM
• Phone: 805-658-2984
• Email: GEORGENE.AUSTRIA@PARKER.COM
• Phone: 805-658-2984
• Email: GEORGENE.AUSTRIA@PARKER.COM
• Phone: 805-658-2984
• Email: GEORGENE.AUSTRIA@PARKER.COM
• Phone: 805-658-2984
• Email: GEORGENE.AUSTRIA@PARKER.COM
• Phone: 805-658-2984
• Email: GEORGENE.AUSTRIA@PARKER.COM
• Phone: 805-658-2984
• Email: GEORGENE.AUSTRIA@PARKER.COM
• Phone: 805-658-2984
• Email: GEORGENE.AUSTRIA@PARKER.COM
• Phone: 805-658-2984
• Email: GEORGENE.AUSTRIA@PARKER.COM
• Phone: 805-658-2984
• Email: GEORGENE.AUSTRIA@PARKER.COM
• Phone: 805-658-2984
• Email: GEORGENE.AUSTRIA@PARKER.COM
• Phone: 805-658-2984
• Email: GEORGENE.AUSTRIA@PARKER.COM

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B249VA002191 [Primary]
HIBCC	VA00219 [Unit of Use]
HIBCC	VA002191 [Package]; Package: BOX [25 Units]; In Commercial Distribution

FDA Product Code

• HFM: Monitor, Uterine Contraction, External (For Use In Clinic)

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: 2016-08-18

On-Brand Devices [FEATHERLITE AQUA]

• B249VA002191: SUBMERSIBLE TOCODYNAMOMETER TRANSDUCER
• B249VA002190: SUBMERSIBLE TOCODYNAMOMETER TRANSDUCER