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Philips Avent Double Breast Pump Kit

FDA UDI

Class II (US FDA UDI)

by Philips Consumer Lifestyle B.V.

Identity

Trade Name
Philips Avent Double Breast Pump Kit FDA UDI
Generic Name
Breast pump, electric FDA UDI
Device Name
INCLUDES: 2X PUMP BODY, 2X SILICONE TUBE AND CAP, 2X SILICONE DIAPHRAGM, 2X CUSHION, 2X WHITE VALVE, 2X 4 FL.0Z. (125ML) BOTTLE, 2X SCREW RING, 2X SEALING DISC FDA UDI
Model / Reference
SCF338/52 FDA UDI
Description
INCLUDES: 2X PUMP BODY, 2X SILICONE TUBE AND CAP, 2X SILICONE DIAPHRAGM, 2X CUSHION, 2X WHITE VALVE, 2X 4 FL.0Z. (125ML) BOTTLE, 2X SCREW RING, 2X SEALING DISC FDA UDI

Identifiers

Catalog Number
SCF338/52 FDA UDI
Primary DI / UDI-DI
00075020107770 FDA UDI
510(k) Number
K203383 FDA UDI
FDA Product Code
HGX FDA UDI
GMDN Term
Breast pump, electric FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
884.5160 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

No

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

No

FDA UDI

Manufacturing Date

Yes

FDA UDI

Category: Breast pump, electric

Philips Avent Double Breast Pump Kit by Philips Consumer Lifestyle B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Breast pump, electric.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 2aacf76b-55eb-4732-8025-a8db1d77f5cc 35 fields · synced Sep 18, 2026