Identity
- Trade Name
- Philips Avent Manual Breast Pump FDA UDI
- Generic Name
- Breast pump, manual FDA UDI
- Device Name
- The Philips Avent Manual Breast Pump consists of: - a pump handle which is squeezed by the user to suction milk from the breast - a breast shield wich is centered over the nipple - a milk container which collect the milk as it is pumped from the breast The Philips Avent Manual Breast Pump is intended to express and collect milk from the breast of a lactating woman. The device is intended for a single user. FDA UDI
- Model / Reference
- SCF430/30 FDA UDI
- Description
- The Philips Avent Manual Breast Pump consists of: - a pump handle which is squeezed by the user to suction milk from the breast - a breast shield wich is centered over the nipple - a milk container which collect the milk as it is pumped from the breast The Philips Avent Manual Breast Pump is intended to express and collect milk from the breast of a lactating woman. The device is intended for a single user. FDA UDI
Identifiers
- Catalog Number
- SCF430/30 FDA UDI
- Primary DI / UDI-DI
- 00075020096753 FDA UDI
- FDA Product Code
- HGY FDA UDI
- GMDN Term
- Breast pump, manual FDA UDI
Classification
- Device Class
- Class I FDA UDI
- Regulation Number
- 884.5150 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
Yes
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, manual
Philips Avent Manual Breast Pump by Philips Consumer Lifestyle B.V. — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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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 I | Pending data |
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Manufacturer
- Manufacturer
- Philips Consumer Lifestyle B.V.
Sources (1)
- FDA UDI a1210066-d0f3-4eca-9cf6-d3ca5ea341d2 34 fields · synced Sep 18, 2026