Identity
- Trade Name
- ipsogen® JAK2 RGQ PCR Kit FDA UDI
- Generic Name
- JAK2 V617F gene mutation IVD, kit, nucleic acid technique (NAT) FDA UDI
- Model / Reference
- V1 FDA UDI
Identifiers
- Catalog Number
- 673633 FDA UDI
- Primary DI / UDI-DI
- 04053228015444 FDA UDI
- 510(k) Number
- DEN160028 FDA UDI
- FDA Product Code
- PSU FDA UDI
- GMDN Term
- JAK2 V617F gene mutation IVD, kit, nucleic acid technique (NAT) FDA UDI
Classification
- Device Class
- Class II FDA UDI
- Regulation Number
- 866.6070 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
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: JAK2 V617F gene mutation IVD, kit, nucleic acid technique (NAT)
ipsogen® JAK2 RGQ PCR Kit by Qiagen, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
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
- Qiagen, Inc.
Sources (1)
- FDA UDI fa80cd90-2364-441f-b62b-02e7b1f960d9 34 fields · synced May 31, 2026