Primary Device ID | 00075020063823 |
NIH Device Record Key | 5bfae09b-7243-4cca-9824-b302dad93e6c |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Philips Avent Breast Pump Double |
Version Model Number | SCF334 |
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 | 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 | true |
Device Issuing Agency | Device ID |
---|---|
GS1 | 00075020063823 [Primary] |
HGX | PUMP, BREAST, POWERED |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | Update |
Device Record Status | Published |
Public Version Number | 2 |
Public Version Date | 2018-03-29 |
Device Publish Date | 2016-09-17 |
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