Identity
- Trade Name
- FastPack® IP hCG Kit (30) FDA UDI
- Generic Name
- Total human chorionic gonadotropin IVD, kit, chemiluminescent immunoassay FDA UDI
- Device Name
- 30 Test Ported hCG Immunoassay Kit FDA UDI
- Model / Reference
- hCG Immunoassay FDA UDI
- Description
- 30 Test Ported hCG Immunoassay Kit FDA UDI
Identifiers
- Catalog Number
- 25000044 FDA UDI
- Primary DI / UDI-DI
- 10816467020126 FDA UDI
- 510(k) Number
- K072264 FDA UDI
- FDA Product Code
- JHI FDA UDI
- GMDN Term
- Total human chorionic gonadotropin IVD, kit, chemiluminescent immunoassay FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 862.1155 FDA UDI
- Commercial Distribution
- In Commercial Distribution FDA UDI
Clinical & Handling
Sterile
No
FDA UDI
Single Use
Yes
FDA UDI
Implantable
No
FDA UDI
Contains Latex
No
FDA UDI
Prescription Use
Yes
FDA UDI
Over-the-Counter
No
FDA UDI
Convenience Kit
Yes
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
No
FDA UDI
Expiration Date
Yes
FDA UDI
Manufacturing Date
No
FDA UDI
Category: Total human chorionic gonadotropin IVD, kit, chemiluminescent immunoassay
FastPack® IP hCG Kit (30) by Qualigen Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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Also classified as Total human chorionic gonadotropin IVD, kit, chemiluminescent immunoassay.
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- iFlash-HCG — Shenzhen YHLO Biotech Co., Ltd. · Class II
Cleared under the same submission
K072264 also covers:
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 |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Qualigen Inc.
Sources (1)
- FDA UDI e192cea2-7bd5-442f-88fa-13892b909d7f 37 fields · synced May 30, 2026