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Lansinoh Manual Breast Pump
FDA UDIClass I (US FDA UDI)
by Lansinoh Laboratories Saglik Gerecleri Tasarim Sanayi Ticaret Ltd Sti
Identity
- Trade Name
- Lansinoh Manual Breast Pump FDA UDI
- Generic Name
- Breast pump, manual FDA UDI
- Device Name
- The Non-Powered Breast Pump is intended to express and collect the breast milk of a nursing woman for the purpose of feeding the collected milk to a baby. FDA UDI
- Model / Reference
- MBP 1.0 FDA UDI
- Description
- The Non-Powered Breast Pump is intended to express and collect the breast milk of a nursing woman for the purpose of feeding the collected milk to a baby. FDA UDI
Identifiers
- Catalog Number
- 50520 FDA UDI
- Primary DI / UDI-DI
- 20044677505202 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
No
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
No
FDA UDI
Serial Number
No
FDA UDI
Expiration Date
No
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Breast pump, manual
Lansinoh Manual Breast Pump by Lansinoh Laboratories Saglik Gerecleri Tasarim Sanayi Ticaret Ltd Sti — Class I — FDA UDI — listed in FDA GUDID
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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
Sources (1)
- FDA UDI 5102df6a-b683-4313-921f-83bddb1e186b 35 fields · synced May 29, 2026