Primary Device ID | 00075020107756 |
NIH Device Record Key | b016939c-8b8d-4a71-8c52-c48ccf1ffd87 |
Commercial Distribution Status | In Commercial Distribution |
Brand Name | Philips Avent |
Version Model Number | SCF393/82 |
Catalog Number | SCF393/82 |
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 |