Primary Device ID | 00075020086655 |
NIH Device Record Key | aa983e5c-5f78-4156-bd61-7f9bb7ef95d3 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Philips Avent Single electric breast pump Advanced |
Version Model Number | SCF392/62 |
Catalog Number | SCF392/62 |
Company DUNS | 489122720 |
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 | true |
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 | 00075020086655 [Primary] |
HGX | Pump, Breast, Powered |
Steralize Prior To Use | false |
Device Is Sterile | false |
Public Version Status | New |
Device Record Status | Published |
Public Version Number | 1 |
Public Version Date | 2020-12-25 |
Device Publish Date | 2020-12-17 |
00075020091499 | Powered breast pump consisting of a motor unit with a press-button user interface, and 1 express |
00075020091482 | Powered breast pump consisting of a motor unit with a press-button user interface, and 1 express |
00075020089724 | Powered breast pump consisting of a motor unit with a press-button user interface, and 1 express |
00075020086655 | Powered breast pump consisting of a motor unit with a press-button user interface, and 1 express |