Identity
- Trade Name
- PathVysion FDA UDI
- Generic Name
- Human epidermal growth factor receptor 2 (HER2) protein IVD, reagent FDA UDI
- Device Name
- PathVysion HER-2 DNA Probe Kit FDA UDI
- Model / Reference
- 02J01-030 FDA UDI
- Description
- PathVysion HER-2 DNA Probe Kit FDA UDI
Identifiers
- Catalog Number
- 02J01-030 FDA UDI
- Primary DI / UDI-DI
- 00884999001732 FDA UDI
- PMA Number
- P980024 FDA UDI
- FDA Product Code
- MVD FDA UDI
- GMDN Term
- Human epidermal growth factor receptor 2 (HER2) protein IVD, reagent FDA UDI
Classification
- Device Class
- Class III 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: Human epidermal growth factor receptor 2 (HER2) protein IVD, reagent
PathVysion by Abbott Molecular — Class III — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS
Similar devices
Also classified as Human epidermal growth factor receptor 2 (HER2) protein IVD, reagent.
- PathVysion — Abbott Molecular · Class III
- PathVysion — Abbott Molecular · Class III
Cleared under the same submission
P980024 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 III | Pending data |
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Manufacturer
- Manufacturer
- Abbott Molecular
Sources (1)
- FDA UDI 4fb5db1f-002f-4a9d-a768-42fabe46a008 37 fields · synced May 29, 2026