Identity
- Trade Name
- Evert-It FDA UDI
- Generic Name
- Breast pump, manual FDA UDI
- Device Name
- Evert-It Nipple Enhancer FDA UDI
- Model / Reference
- 36000 FDA UDI
- Description
- Evert-It Nipple Enhancer FDA UDI
Identifiers
- Catalog Number
- 36000 FDA UDI
- Primary DI / UDI-DI
- 00683693360004 FDA UDI
- 510(k) Number
- K962828 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
No
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
Evert-It by Mai/Genesis — 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
- Mai/Genesis
Sources (1)
- FDA UDI 1938d6bf-9a2c-4718-8d8a-3cd74358f2c1 35 fields · synced Jun 8, 2026