| 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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