Identity
- Trade Name
- Philips Avent Single Electric Breast Pump FDA UDI
- Generic Name
- Breast pump, electric FDA UDI
- Device Name
- SCF332/21 FDA UDI
- Model / Reference
- SCF332/21 FDA UDI
- Description
- SCF332/21 FDA UDI
Identifiers
- Catalog Number
- SCF332/21 FDA UDI
- Primary DI / UDI-DI
- 00075020070074 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
- Not 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
No
FDA UDI
Philips Avent Single Electric Breast Pump by Philips Consumer Lifestyle B.V. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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 |
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Manufacturer
- Manufacturer
- Philips Consumer Lifestyle B.V.
Sources (1)
- FDA UDI 69cae5fc-6c63-4165-80c1-a69c980cb9b9 35 fields · synced Sep 18, 2026