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 Issuing Agency | Device ID |
---|---|
GS1 | 00007502005175 [Primary] |
GS1 | 20075020050858 [Package] Contains: 00007502005175 Package: [6 Units] Discontinued: 2018-09-26 Not in Commercial Distribution |
NUH | STIMULATOR, NERVE, TRANSCUTANEOUS, OVER-THE-COUNTER |
Steralize Prior To Use | false |
Device Is Sterile | false |
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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