Identity
- Trade Name
- Philips Avent Double Electric Breast Pump FDA UDI
- Generic Name
- Breast pump, electric FDA UDI
- Device Name
- ME motor unit Qty: 1 - 2k expression kit (Body) Qty: 2 - Nat 3.0 bottle Qt:2 - Teat Qty:1 - Screw ring Qty: 2 - Sealing Disc Qty:1 - Bottle Cap Qty: 1 - Travel Bag Qty: 1 - Insulation pouch Qty: 1 FDA UDI
- Model / Reference
- SCF393/82 FDA UDI
- Description
- ME motor unit Qty: 1 - 2k expression kit (Body) Qty: 2 - Nat 3.0 bottle Qt:2 - Teat Qty:1 - Screw ring Qty: 2 - Sealing Disc Qty:1 - Bottle Cap Qty: 1 - Travel Bag Qty: 1 - Insulation pouch Qty: 1 FDA UDI
Identifiers
- Catalog Number
- SCF393/82 FDA UDI
- Primary DI / UDI-DI
- 00075020107756 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 Double Electric Breast Pump by Philips Consumer Lifestyle B.V. — Class II — 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 II | Pending data |
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Manufacturer
- Manufacturer
- Philips Consumer Lifestyle B.V.
Sources (1)
- FDA UDI b016939c-8b8d-4a71-8c52-c48ccf1ffd87 34 fields · synced Sep 18, 2026