Identity
- Trade Name
- Conception Kit FDA UDI
- Generic Name
- Natural conception assistance kit FDA UDI
- Device Name
- Lot number, Expiration Date, Individual Kit Number, Temperature Range and the statement: The Conception Kit should be kept away from direct sunlight, moisture and heat. FDA UDI
- Model / Reference
- CX-0002-ML EN/ES FDA UDI
- Description
- Lot number, Expiration Date, Individual Kit Number, Temperature Range and the statement: The Conception Kit should be kept away from direct sunlight, moisture and heat. FDA UDI
Identifiers
- Catalog Number
- CX-0002-ML EN/ES FDA UDI
- Primary DI / UDI-DI
- 00895863001000 FDA UDI
- FDA Product Code
- OBB FDA UDI
- GMDN Term
- Natural conception assistance kit FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 884.5250 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
Yes
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
Yes
FDA UDI
Serial Number
Yes
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
Yes
FDA UDI
Category: Natural conception assistance kit
Conception Kit by Conceivex, Inc. — 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
- Conceivex, Inc.
Sources (1)
- FDA UDI f4f509b2-c2d8-4952-80c6-fc6b66397f49 37 fields · synced May 31, 2026