Philips Avent

GUDID 00075020070104

SCF334/25 F-Box

Philips Consumer Lifestyle B.V.

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Primary Device ID00075020070104
NIH Device Record Keydf944809-4126-4676-aaf2-57e7916c6260
Commercial Distribution StatusIn Commercial Distribution
Brand NamePhilips Avent
Version Model NumberSCF334
Company DUNS491996556
Company NamePhilips Consumer Lifestyle B.V.
Device Count1
DM Exempttrue
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Countertrue

Device Identifiers

Device Issuing AgencyDevice ID
GS100075020070104 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HGXPUMP, BREAST, POWERED

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2017-09-17

On-Brand Devices [Philips Avent]

00075020070111SCF334/26 F-Box
00075020070104SCF334/25 F-Box
00075020070098SCF334/23 F-Box
00075020070081SCF334/22 F-Box
00075020070074SCF332/21 F-Box
00075020107756ME motor unit Qty: 1 - 2k expression kit (Body) Qty: 2 - Nat 3.0 bottle Qt:2 - Teat Qty:1 -

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