Primary Device ID | 00075020070098 |
NIH Device Record Key | 9fe4b51b-ff41-493b-85e6-6620be298274 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Philips Avent |
Version Model Number | SCF334 |
Company DUNS | 491996556 |
Company Name | Philips Consumer Lifestyle B.V. |
Device Count | 1 |
DM Exempt | true |
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 |