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Philips Avent Single electric breast pump Advanced
FDA UDIClass II (US FDA UDI)
Identity
- Trade Name
- Philips Avent Single electric breast pump Advanced FDA UDI
- Generic Name
- Breast pump, electric FDA UDI
- Device Name
- Powered breast pump consisting of a motor unit with a press-button user interface, and 1 expression kit (Cushion-type) with 1 milk collection container. With a rechargeable battery. FDA UDI
- Model / Reference
- SCF392/61 FDA UDI
- Description
- Powered breast pump consisting of a motor unit with a press-button user interface, and 1 expression kit (Cushion-type) with 1 milk collection container. With a rechargeable battery. FDA UDI
Identifiers
- Catalog Number
- SCF392/61 FDA UDI
- Primary DI / UDI-DI
- 00075020091499 FDA UDI
- 510(k) Number
- K201381 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
Yes
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
Yes
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Breast pump, electric
Philips Avent Single electric breast pump Advanced by Philips Consumer Lifestyle B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Cleared under the same submission
K201381 also covers:
- Philips Avent Double electric breast pump Advanced — Philips Consumer Lifestyle B.V.
- Philips Avent Double electric breast pump Advanced — Philips Consumer Lifestyle B.V.
- Philips Avent Single electric breast pump Advanced — Philips Consumer Lifestyle B.V.
- Philips Avent Single electric breast pump Advanced — Philips Consumer Lifestyle B.V.
- Philips Avent Single electric breast pump Advanced — Philips Consumer Lifestyle B.V.
Authorization Coverage (1 country)
Regulatory Authorizations
United States Pending data
FDA UDI
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA UDI | United States | FDA UDI | Registered in GUDID | Class II | Pending data |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Philips Consumer Lifestyle B.V.
Sources (1)
- FDA UDI 26a63551-8567-4758-9146-2a7121d18a3f 36 fields · synced Sep 18, 2026