989803143931

GUDID 00884838009974

Philips Medizin Systeme Böblingen GmbH

Intrapartum pressure monitoring catheter

• Primary Device ID: 00884838009974
• NIH Device Record Key: 633d01ea-b930-44d9-b6b4-f72b14b0325b
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: 989803143931
• Catalog Number: 989803143931
• Company DUNS: 314101143
• Company Name: Philips Medizin Systeme Böblingen GmbH
• 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: false
• 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(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx
• Phone: +1(999)999-9999
• Email: xx@xx.xx

Device Identifiers

Device Issuing Agency	Device ID
GS1	00884838009974 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K140535

FDA Product Code

• DSA: CABLE, TRANSDUCER AND ELECTRODE, PATIENT, (INCLUDING CONNECTOR)

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: false

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-11-17

Devices Manufactured by Philips Medizin Systeme Böblingen GmbH

• 00884838117433 - NOUN: 2026-03-27 24" patient cable, for use only with the DigiTrak XT recorder,
• 00884838113770 - MR Patient Care Adult SpO2 Clip: 2026-03-24 Reusable SpO2 finger clip designed for use with the Quick Connect SPO2 Sensor (989803161991) - Sized for Adult patients
• 00884838100978 - MR Patient Care Pediatric SpO2 Clip: 2026-03-24 Reusable SpO2 finger clip designed for use with the Quick Connect SPO2 Sensor (989803161991) - Sized for Pediatric patients
• 00884838128880 - Patient Information Center iX: 2026-03-17 Patient Information Center iX
• 00884838129214 - Care Assist: 2026-03-17 Care Assist
• 00884838129221 - Care Assist: 2026-03-17 Care Assist
• 00884838117877 - MR Patient Care Pediatric SpO2 Clip: 2026-03-17 Reusable SpO2 finger clip designed for use with the Quick Connect SPO2 Sensor (989803161991) - Sized for Pediatric patients
• 00884838117358 - patient lead wire: 2026-03-13 Std 10-lead Patient Cable IEC