Philips PulseRelief

GUDID 20075020050858

Philips Consumer Lifestyle B.V.

Physical therapy transcutaneous neuromuscular electrical stimulation system

• Primary Device ID: 20075020050858
• NIH Device Record Key: 0714cca4-8a38-466f-b35a-53af5ab60fb0
• Commercial Distribution Discontinuation: 2017-12-01
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: Philips PulseRelief
• Version Model Number: PR3841
• Company DUNS: 491996556
• Company Name: Philips Consumer Lifestyle B.V.
• 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: true
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: true

Device Identifiers

Device Issuing Agency	Device ID
GS1	00007502005175 [Primary]
GS1	20075020050858 [Package]; Contains: 00007502005175; Package: [6 Units]; Discontinued: 2018-09-26; Not in Commercial Distribution

FDA Product Code

• NUH: STIMULATOR, NERVE, TRANSCUTANEOUS, OVER-THE-COUNTER

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 5
• Public Version Date: 2019-10-23
• Device Publish Date: 2016-08-24

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